Pyrimidine derivatives exhibiting antitumor activity

ABSTRACT

A compound represented by the formula (I):                    
     wherein, for example, R 1 , R 2 , R 3 , and R 4  are each independently hydrogen atom, alky, and the like, R 5  and R 6  are each independently hydrogen atom, alkyl, and the like, X is —O—, —S—, and the like, Y is 5-membered heteroaryl-diyl and the like, Z is optionally substituted aryl and the like, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates.

This application is the national phase under 35 U.S.C. §371 of PCT International Application No. PCT/JP99/03863 which has an International filing date of Jul. 16, 1999, which designated the United States of America.

TECHNICAL FIELD

The present invention relates to a novel pyrimidine derivative having an antitumor activity, a cytostatic activity, and an inhibitory activity against a signal derived from Ras oncogene products.

BACKGROUND ART

The oncogene “ras” such as H-ras, K-ras, and N-ras is mutated and activated in many of neoplasms. The “Ras”, the products of ras oncogene, strongly concerns tumorigenesis caused by acceleration of cell cycle and induction of expression of many of genes associated with a malignant conversion such as a vascular endothelial growth factor and type-IV coliagenase. Especially, it is found that there is highly frequent ras mutation in solid tumor such as pancreatic cancer (>80%), colon cancer (>40%), and lung cancer (>20%) which are difficult to be cured by using existing chemotherapeutics. Therefore, it is considered that Ras is one of the most important target molecules in the development of the chemotherapeutics against them.

A farnesyl-protein-transferase (FPT) inhibitor (FPTI) is known as chemotherapeutics of which target are Ras (WO95/13059, WO95/25086, WO95/25092, W095134535, U.S. Pat. No. 5,608,067, and JP-A-7-112930).

In the cells expressing activated Ras, the excess signals reach cell nucleus through some signaling pathways and some signal transmitter molecules such as MAPK (Mitogen Activated Protein Kinase) and P13K (Phosphatidylinositol-3-Kinase). The signals activate the transcription factors such as AP1 (Activator Protein-1) and ETS (E26 transformation specific) in the cell nucleus and then they induce the expression of many genes related to malignant features through transcription activation element such as Ras Responsive Element (RRE). Therefore, it is possible to repress the malignant conversion of the cancer cells, when the signal transmission (a signal derived from ras oncogene products) is inhibited.

DISCLOSURE OF INVENTION

In the above situation, the inventors of the present invention have studied on the antitumor agent having an inhibitory activity against a signal derived from Ras oncogene products.

The activation of gene expression through RRE is in proportion to a signal derived from Ras and the signal can be measured by the amount of its expression. The inventors of the present invention artificially made cells having activated Ras wherein expression of firefly luciferase gene, reporter gene, is regulated by RRE and carried out a screening of the inhibitors taking luciferase activity shown by the cells as an index of signals through Ras. As a result, the inventors of the present invention found that a series of pyrimidine derivatives have a strong inhibitory activity against a signal derived from Ras oncogene products.

The present invention relates to I) a compound represented by the formula (I):

wherein R¹, R², R³, and R⁴ are each independently hydrogen atom, optionally substituted alky, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, an optionally substituted non-aromatic heterocyclic group, or acyl; or

R¹ and R², R³ and R⁴, and R² and R³ each taken together with the adjacent nitrogen atom form the same or different 3- to 6-membered ring optionally containing O, S, or N, provided that R¹ and R² and R³ and R⁴ do not form a ring when R² and R³ taken together form a ring;

R⁵ and R⁶ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkyloxy, alkylthio, optionally substituted alkyloxycarbonyl, optionally substituted aryl, optionally substituted heteroaryl, halogen, hydroxy, mercapto, optionally substituted amino, carboxy, cyano, or nitro;

X is —N(R⁷)—, —NH—NH—, —O—, or —S— wherein R⁷ is hydrogen atom or optionally substituted alkyl;

Y is optionally substituted 5-membered non-aromatic heterocycle-diyl or optionally substituted 5-membered heteroaryl-diyl;

Z is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aryl alkenyl, or optionally substituted alkenyl; the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates.

In more detail, the present invention relates to:

II) a compound represented by the formula (II):

 wherein R⁸, R⁹, R¹⁰, and R¹¹ are each independently hydrogen atom, optionally substituted alkyl, alkenyl, alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, a non-aromatic heterocyclic group, or acyl;

W is —O—, —S—, or —N(R^(A))— wherein R^(A) is hydrogen atom or optionally substituted alkyl;

R⁵, R⁶, X, and Z are as defined above, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates,

III) a compound represented by the formula (III):

 wherein R⁵, R⁶, R⁸, R⁹, R¹⁰, R¹¹, and Z are as defined above, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates,

IV) a compound represented by the formula (IV):

 wherein R¹² is hydrogen atom or alkyl;

V is optionally substituted aryl;

R⁸, R⁹, R¹⁰, and R¹¹ are as defined above, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates,

V) a compound, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates as described in above I), wherein R¹, R², R³, and R⁴ are each independently hydrogen atom, optionally substituted alkyl, alkenyl, alkynyl, or acyl,

VI) a compound, the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates as described in any one of the above II) to IV), wherein R⁸, R⁹, R¹⁰, and R¹¹ are each independently hydrogen atom, optionally substituted alkyl, alkenyl, alkynyl, or acyl,

VII) a pharmaceutical composition which contains as active ingredient a compound as described in any one of I) to VI),

VIII) a pharmaceutical composition for use as an antitumor agent which contains as active ingredient a compound as described in any one of I) to VI)s,

IX) a pharmaceutical composition for use as a cytostatic agent which contains as described in any one of I) to VI),

X) a pharmaceutical composition for use as an inhibitor against a signal derived from Ras oncogene products which contains as active ingredient a compound as described in any one of I) to VI),

XI) use of a compound of any one of I) to VI) for the preparation of a pharmaceutical composition for treating cancer, and

XII) a method of treating a mammal, including a human, to alleviate the pathological effects of cancer; which comprises administration to the mammal of a compound as described in any one of I) to VI).

The term “alkyl” employed alone or in combination with other terms in the present specification includes a straight or branched chain monovalent hydrocarbon group having 1 to 8 carbon atoms. Examples of the alkyl include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, isohexyl, n-heptyl, n-octyl and the like. Preferably, C1 to C6 alkyl is exemplified. More preferably, C1 to C3 alkyl is exemplified.

The term “alkenyl” employed alone or in combination with other terms in the present specification includes a straight or branched chain monovalent hydrocarbon group having 2 to 8 carbon atoms and one or more double bonds. An example of the alkenyl includes vinyl, allyl, propenyl, crotonyl, prenyl, a variety of butenyl isomers and the like. Preferably, C2 to C6 alkenyl is exemplified. More preferably, C2 to C3 alkenyl is exemplified.

The term “alkynyl” employed alone or in combination with other terms in the present specification includes a straight or branched chain monovalent hydrocarbon group having 2 to 8 carbon atoms and one or more triple bonds. The alkynyl may contain (a) double bond(s). An example of the alkenyl includes ethynyl, propynyl, 6-heptynyl, 7-octynyl, and the like. Preferably, C2 to C6 alkynyl is exemplified. More preferably, C2 to C3 alkynyl is exemplified.

The term “aryl” employed alone or in combination with other terms in the present specification includes a monocyclic or condensed cyclic aromatic hydrocarbon. An example of the aryl includes phenyl, 1-naphthyl, 2-naphthyl, anthryl and the like. Preferably, phenyl, 1-naphthyl, and 2-naphthyl are exemplified. More preferably, phenyl is exemplified.

The term “aralkyl” in the present specification includes a group wherein the above-mentioned “alkyl” is substituted with the above-mentioned “aryl”. An example of aralkyl includes benzyl, phenethyl (e.g., 2-phenylethyl), phenylpropyl (e.g., 3-phenylpropyl), naphthylmethyl (e.g., 1-naphthylmethyl and 2-naphthylmethyl), anthrylmethyl (e.g., 9-anthrylmethyl) and the like. Preferably, benzyl and phenylethyl are exemplified.

The term “heteroaryl” employed alone or in combination with other terms in the present specification includes a 5- to 6-membered aromatic cyclic group which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms in the ring and may be fused with the above mentioned “aryl”, “heteroaryl”, “carbocyclic group”, and “non-aromatic heterocyclic group”. Heteroaryl is bonded at any possible position when the heteroaryl is a condensed ring. Examples of the heteroaryl are pyrrolyl (e.g., 1-pyrrolyl), indolyl (e.g., 3-indolyl), carbazolyl (e.g., 3-carbazolyl), imidazolyl (e.g., 4- imidazolyl), pyrazolyl (e.g., 3-pyrazolyl and 5-pyrazolyl), benzimidazolyl (e.g., 2-benzimidazolyl), indazolyl (e.g., 3-indazolyl), indolizinyl (e.g., 6-indolizinyl), pyridyl (e.g., 3-pyridyl and 4-pyridyl), quinolyl (e.g., 5-quinolyl), isoquinolyl (e.g., 3-isoquinolyl), acridinyl (e.g., 1-acridinyl), phenanthridinyl (e.g., 2-phenanthridinyl), pyridazinyl (e.g., 3-pyridazinyl), pyrimidinyl (e.g., 4-pyrimidinyl), pyrazinyl (e.g., 2-pyrazinyl), cinnolinyl (e.g., 3-cinnolinyl), phthalazinyl (e.g., 2-phthalazinyl), quinazolinyl (e.g., 2-quinazolinyl), isoxazolyl (e.g., 3-isoxazolyl), benzisoxazolyl (e.g., 3-benzisoxazolyl), oxazolyl (e.g., 2-oxazolyl), benzoxazolyl (e.g., 2-benzoxazolyl), benzoxadiazolyl (e.g., 4-benzoxadiazolyl), isothiazolyl (e.g., 3-isothiazolyl), benzisothiazolyl (e.g., 2-benzisothiazolyl), thiazolyl (e.g., 4-thiazolyl), benzothiazolyl (e.g., 2-benzothiazolyl), furyl (e.g., 2-furyl and 3-furyl), benzofuryl (e.g., 3-benzofuryl), thienyl (e.g., 2-thienyl and 3-thienyl), benzothienyl (e.g., 2-benzothienyl), tetrazolyl, oxadiazolyl (e.g., 1,3,4-oxadiazolyl and 1,2,4-oxadiazolyl), oxazolyl, thiadiazolyl (e.g., 1,3,4-thiadiazolyl and 1,2,4-thiadiazolyl), 4H-1,2,4-triazolyl, quinoxalinyl, 2-pyridone-3-yl, and the like. Preferably, pyridyl, pyrazinyl, furyl, thienyl and the like are exemplified.

The term “5-membered heteroaryl-diyl” herein used includes a 5-membered divalent group derived from above-mentioned “heteroaryl”. Examples of the 5-membered heteroaryl-diyl are 2,5-furandiyl, 2,5-thiophendiyl, 2,5-pyrroldiyl, 3,5-pyrazoldiyl, 2,5-(1,3,4-oxadiazole)diyl, 3,5-(1,2,4-oxadiazole)diyl, 2,5-oxazoldiyl, 3,5-isoxazoldiyl, 2,5-(1,3,4-thiadiazole)diyl, 3,5-(1,2,4-thiadiazole)diyl, 3,5-(4H-1,2,4-triazole)diyl, and the like.

The term “non-aromatic heterocyclic group” employed alone or in combination with other terms in the present specification includes a 5- to 7-membered non-aromatic heterocyclic group which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms in the ring and a cyclic group wherein two or more of the above-mentioned heterocyclic groups are fused. Examples of the heterocyclic group are pyrrolidinyl (e.g., 1-pyrrolidinyl), pyrazolidinyl (e.g., 1-pyrazolidinyl), piperidinyl (e.g., piperidino and 2-piperidinyl), piperazinyl (e.g., 1-piperazinyl), morpholinyl (e.g., morpholino and 3-morpholinyl), and the like.

The term “5-membered non-aromatic heterocycle-diyl” herein used includes a 5-membered divalent group derived from the above-mentioned “non-aromatic heterocyclic group”. Examples of the 5-membered non-aromatic heterocycle-diyl are pyrrolidindiyl (e.g., 2,5-pyrrolidindiyl) and the like.

The term “carbocyclic group” herein used includes a 3- to 7-membered non-aromatic carbocyclic group. Examples of the carbocyclic group are cycloalkyl (e.g., cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl), cycloalkenyl (e.g., cyclopentenyl and cyclohexenyl), and the like.

In this specification, examples of the ring represented by “R¹ and R², R³ and R⁴, and R² and R³ each taken together with the adjacent nitrogen atom form the same or different 3- to 6-membered non-aromatic heterocyclic ring” are aziridine, pyrrolidine, piperidine, piperazine, morpholine, imidazolidine, pyrazolidine, pyrrole, py dine, triazine, and the like.

The term “acyl” employed alone or in combination with other terms in the present specification includes alkylcarbonyl of which alkyl part is the above-mentioned “alkyl” and arylcarbonyl of which aryl part is the above-mentioned “aryl”. Examples of the acyl are acetyl, propanoyl, benzoyl, and the like.

The term “halogen” herein used means fluoro, chloro, bromo, and iodo.

Examples of “alkyloxy” herein used are methyloxy, ethyloxy, n-propyloxy, isopropyloxy, n-butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, and the like. Preferably, methyloxy, ethyloxy, n-propyloxy, and isopropyloxy are exemplified.

Examples of “alkylthio” herein used are methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio, tert-butylthio, and the like. Preferably, methylthio, ethylthio, n-propylthio, and isopropylthio are exemplified.

Examples of “alkyloxycarbonyl” herein used are methyloxycarbonyl, ethyloxycarbonyl, n-propyloxycarbonyl, and the like.

The term “optionally substituted amino” herein used means amino substituted with one or two of the above-mentioned “alkyl”, “aralkyl”, “acyl”, optionally substituted sulfonyl (e.g., alkyloxyphenylsulfonyl), arylalkylene (e.g., benzylidene), alkylsulfonyl, carbamoyl and the like or non-substituted amino. Examples of the optionally substituted amino are amino, methylamino, ethylamino, dimethylamino, ethylmethylamino, diethylamino, benzylamino, benzoylamino, acetylamino, propionylamino, tert-butyloxycarbonylamino, benzylidenamino, methylsulfonylamino, 4-methoxyphenylsulfonylamino, and the like. Preferably, amino, methylamino, dimethylamino, diethylamino, acetylamino are exemplified.

Substituentson the aromatic ring of “optionally substituted aralkyl” are, for example, hydroxy, alkyloxy (e.g., methyloxy and ethyloxy), mercapto, alkylthio (e.g., methylthio), cycloalkyl (e.g., cyclopropyl, cyclobutyl, and cyclopentyl), halogen (e.g., fluoro, chloro, bromo, and iodo), carboxy, alkyloxycarbonyl (e.g., methyloxycarbonyl and ethyloxycarbonyl), nitro, cyano, haloalkyl (e.g., trifluoromethyl), aryloxy (e.g., phenyloxy), optionally substituted amino (e.g., amino, methylamino, dimethylamino, diethylamino, and benzylidenamino), alkyl (e.g., methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, and neopentyl), alkenyl (e.g., vinyl and propenyl), alkynyl (e.g., ethynyl and phenylethynyl), formyl, lower alkanoyl (e.g., acetyl and propionyl), acyloxy (e.g., acetyloxy), acylamino, alkylsulfonyl (e.g., methylsulfonyl), and the like. These substituents may be substituted at one or more possible position(s).

Substituents of “optionally substituted alkyl”, “optionally substituted alkyloxy”, and “optionally substituted alkyloxycarbonyl” are, for example, hydroxy, alkyloxy (e.g., methyloxy and ethyloxy), mercapto, alkylthio (e.g., methylthio), cycloalkyl (e.g., cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl), halogen (e.g., fluoro, chloro, bromo, and iodo), carboxy, alkyloxycarbonyl (e.g., methyloxycarbonyl and ethyloxycarbonyl), nitro, cyano, haloalkyl (e.g., trifluoromethyl), optionally substituted amino (e.g., amino, methylamino, dimethylamino, carbamoylamino, and tert-butyloxycarbonylamino), acyloxy (e.g., acetyloxy), optionally substituted aralkyloxy (e.g., benzyloxy and 4-methyloxyphenylmethyloxy), and the like. These substituents may be substituted at one or more possible position(s).

Substituents of “optionally substituted alkenyl” and “optionally substituted alkynyl” are, for example, hydroxy, alkyloxy (e.g., methyloxy and ethyloxy), mercapto, alkylthio (e.g., methylthio), cycloalkyl (e.g., cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl), halogen (e.g., fluoro, chloro, bromo, and iodo), carboxy, alkyloxycarbonyl (e.g., methyloxycarbonyl and ethyloxycarbonyl), nitro, cyano, haloalkyl (e.g., trifluoromethyl), optionally substituted amino (e.g., amino, methylamino, dimethylamino, carbamoylamino, and tert-butyloxycarbonylamino), acyloxy (e.g., acetyloxy), optionally substituted aralkyloxy (e.g., benzyloxy and 4-methyloxyphenylmethyloxy), optionally substituted aryl (e.g., phenyl), and the like. These substituents may be substituted at one or more possible position(s).

The preferable examples of “optionally substituted alkyl” are methyl, ethyl, n-propyl, isopropyl, n-butyl, trifluoromethyl, 2,2,2-trifluoroethyl, hydroxymethyl, cyclohexylmethyl, carboxyethyl, acetyloxyethyl, and benzyloxymethyl. More preferably, methyl, ethyl, n-propyl, isopropyl, n-butyl, trifluoromethyl, 2,2,2-trifluoroethyl are exemplified.

Substituents of “optionally substituted aryl”, “optionally substituted heteroaryl”, “optionally substituted 5-membered heteroaryl-diyl”, “optionally substituted 5-membered non-aromatic heterocycle-diyl”, and “an optionally substituted non-aromatic heterocyclic group” are, for example, hydroxy, optionally substituted alkyloxy (e.g., methyloxy, ethyloxy, n-propyloxy, isopropyloxy, ethyloxycarbonylmethyloxy, carboxymethyloxy and 4-methoxyphenylmethyloxy), mercapto, alkylthio (e.g., methylthio), cycloalkyl (e.g., cyclopropyl, cyclobutyl, cyclopentyl), halogen (e.g., fluoro, chloro, bromo, and iodo), carboxy, alkyloxycarbonyl (e.g., methyloxycarbonyl, ethyloxycarbonyl, and tert-butyloxycarbonyl), nitro, cyano, haloalkyl (e.g., trifluoromethyl), aryloxy (e.g., phenyloxy), optionally substituted amino (e.g., amino, methylamino, dimethylamino, ethylamino, diethylamino, N,N-acetylmethylamino, benzylidenamino, 4-methoxyphenylsulfonylamino, methylsulfonylamino, benzoylamino, acetylamino, propionylarmino, and tert-butyloxycarbonylamino), optionally substituted aminosulfonyl (e.g., aminosulfonyl), optionally substituted alkyl (e.g., methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, t-butyloxycarbonylaminomethyl, and aminomethyl), alkenyl (e.g., vinyl, propenyl, and prenyl), optionally substituted alkynyl (e.g., ethynyl and phenylethynyl), alkenyloxy (e.g., propenyloxy and prenyloxy), formyl, acyl (e.g., acetyl, propionyl, and benzoyl), acyloxy (e.g., acetyloxy), optionally substituted carbamoyl (e.g., carbamoyl and dimethylaminocarbonyl), alkylsulfonyl (e.g., methylsulfonyl), aryl (e.g., phenyl), aralkyl (e.g., benzyl), carbothioamide, optionally substituted heterocyclic group (e.g., dioxolanyl, 2-methyl-1,3-dioxolane-2-yl, pyrrolidinyl, and piperidino), optionally substituted heteroaryl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl, pyridine N-oxide-4-yl, 1-methyl-2-pyridone-4-yl, 1-pyrrolyl, 2-pyrrolyl, and 3-pyrrolyl), and the like. These substituents may be substituted at one or more possible position(s). Preferably, optionally substituted amino, halogen, nitro, alkyl, and alkyloxy are exemplified.

Examples of “optionally substituted aryl” are phenyl, 2-aminophenyl, 3-aminophenyl, 4-aminophenyl, 2-acetylaminophenyl, 4-acetylaminophenyl, 2-benzoylaminophenyl, 4-benzoylaminophenyl, 2-methylsulfonylaminophenyl, 2-propionylaminophenyl, 2-methylaminophenyl, 4-methylaminophenyl, 2-dimethylaminophenyl, 4-dimethylaminophenyl, 2-ethylaminophenyl, 4-ethylaminophenyl, 4-diethylaminophenyl, 2- (4-methoxyphenylsulfonylamino)phenyl, 2-hydroxyphenyl, 4-hydroxyphenyl, 2-ethyloxycarbonylmethyloxyphenyl, 2-carboxymethyloxyphenyl, 2-chlorophenyl, 4-chlorophenyl, 4-bromophenyl, 4-iodophenyl, 4-trifluoromethylphenyl, 2-methylphenyl, 4-methylphenyl, 4-methyloxyphenyl, 4-ethyloxyphenyl, 4-n-propyloxyphenyl, 4-isopropyloxyphenyl, 4-tert-butyloxycarbonylphenyl, 4-prenyloxyphenyl, 2-nitrophenyl, 4-nitrophenyl, 4-(4-methoxyphenylmethyloxy)phenyl, 4-methyloxycarbonylphenyl, 4-aminosulfonylphenyl, 4-(N, N-dimethylaminocarbonyl)phenyl, 4-carboxyphenyl, 4-biphenylyl, 4-benzoylphenyl, 4-pyrrolidinophenyl, 4-piperidinophenyl, 2-(3-amino)naphthyl, 2-amino-5-chlorophenyl, 2-amino-3-chlorophenyl, 2-amino-4-chlorophenyl, 2-amino-6-chlorophenyl, 4-amino-2-chlorophenyl, 2-amino-4-fluorophenyl, 2-amino-5-fluorophenyl, 2-amino-6-fluorophenyl, 4-amino-2-fluorophenyl, 2-amino-4,5-difluorophenyl, 2-amino-3-methylphenyl, 2-amino-4-methylphenyl, 2-amino-5-methylphenyl, 2-amino-6-methylphenyl, 4-amino-3-methylphenyl, 4-amino-3-methyloxyphenyl, 2-amino-4-nitrophenyl, 4-amino-3-hydroxyphenyl, 2-amino-4-carboxyphenyl, 2-amino-4-methyloxycarbonylphenyl, 4-amino-2-hydroxyphenyl, 4-amino-3-(4-methoxyphenylmethyloxy)phenyl, 2, 4-diaminophenyl, 3,4-diaminophenyl, 2-(N-acetyl-N-methylamino)phenyl, 2-acetylamino4-fluorophenyl, 2-acetylamino-4-chlorophenyl, 2,3-dichlorophenyl, 2,4-dichlorophenyl, 2-(3-amino)naphthyl, 4-amino-2-methylphenyl, 2-fluoro-4-nitrophenyl, 4-amino-2-methyloxyphenyl, 2-methyloxy-4-nitrophenyl, 4-fluoro-2-nitrophenyl, 4-amino-2-trifluoromethylphenyl, 4-amino-2-ethyloxyphenyl, 4-amino-2-trifluoromethyloxyphenyl, 2-chloro-4-nitrophenyl, 2-methyl-4-nitrophenyl, 4-nitro-2-trifluoromethyloxyphenyl, 4-nitro-2-trifluoromethylphenyl, 2-ethyloxy-4-nitrophenyl, and the like.

Examples of “optionally substituted heteroaryl” are 3-pyridyl, 3-(2-amino)pyridyl, 5-(2-amino)pyridyl, 2-(3-amino)pyrazinyl, 4-(3-amino)pyrazolyl, 5-(4-amino-2-methyl)pyrimidinyl, 3-(2-amino)thienyl, 2-(3-methyl)thienyl, 2-(5-methyl)thienyl, 2-furyl, 3-furyl, 3-(2-methyl)turyl, 3-(2,5-dimethyl)furyl, 2-(5-bromo)faryl, 4-(2-nitro)furan, 3-(1-methyl-4-nitro)pyrazolyl, 5-(1-methyl-4-nitro)pyrazolyl, 3-(5-nitro)pyrazolyl, 3-(4-nitro)pyyazoyl, 2-(3-pyridyl)-thiazole-4-yl, 2-(4-pyridyl)-thiazole4-yl, 6-(1-pyrrolyl)-pyridine-3-yl, N-methyl-2-pyridone-3-yl, and the like.

Examples of “optionally substituted 5-membered heteroaryl-diyl” are 2,5-flurandiyl, 2,5-thiophendiyl, 2,5-pyrroldiyl, 3,5-pyrazoldiyl, 2,5-(1,3,4-oxadiazole)diyl, 3,5-(1,2,4-oxadiazole)diyl, 2,5-oxazoldiyl, 3,5-isooxazoldiyl, 2,5-(1,3,4-thiadiazole)diyl, 3,5-(1,2,4-thiadiazole)diyl, 3,5-(4H-1,2,4-triazole)diyl, 3,5-(1-methylpyrazole)diyl, and the like.

Examples of “optionally substituted arylalkenyl” are 4-aminophenylethenyl and the like.

Preferable example of R¹ to R⁶, X, Y, and Z of the compound represented by the formula (I) are shown below as groups (a) to (s).

R¹ and R² are (a) each independently hydrogen atom, optionally substituted alky, alkenyl, or alkynyl; (b) each independently hydrogen atom, alkyl optionally substituted with halogen, alkenyl, or alkynyl; and (c) one is hydrogen atom and the other is C1 to C3 alkyl optionally substituted with halogen.

R³ and R⁴ are (d) each independently hydrogen atom, optionally substituted alkyl, alkenyl, or alkynyl; (e) each independently hydrogen atom, alkyl optionally substituted with halogen, alkenyl, or alkynyl; and (f) one is hydrogen atom and the other is C1 to C3 alkyl optionally substituted with halogen.

R⁵ is (g) hydrogen atom, alkyloxy, alkylthio, or optionally substituted alkyl; (h) hydrogen atom or alkyl; and (i) hydrogen or C¹ to C2 alkyl.

R⁶ is (j) hydrogen atom or alkyl; and (k) hydrogen atom.

X is (l) —O— or —S—; and (m) —S—.

Y is (n) 5-membered heteroaryl-diyl; (o) 2,5-(1,3,4-oxadiazole)diyl, 3,5-(1,2,4-oxadiazole)diyl, 2,5-(1,3,4-thiadiazole)diyl, or 3,5-(1,2,4-thiadiazole)diyl; and (p) 2,5-(1,3,4-oxadiazole)diyl.

Z is (q) optionally substituted aryl or optionally substituted heteroaryl; (r) optionally substituted phenyl or optionally substituted monocyclic heteroaryl; and (s) phenyl, pyridyl, thienyl, or furyl, which are substituted with 1 to 3 substituents selected from the group consisting of optionally substituted amino, halogen, alkyl, alkyloxy, acyl, phenyl, alkyloxycarbonyl, hydroxy, nitro, or haloalkyl.

A preferred group of compounds represented by the formula (I) is shown below. [(R¹, R²), (R³, R⁴), R⁵, R⁶, X Y]=[a, d, g, j, l, n], [a, d, g, j, l, o], [a, d, g, j, l, p], [a, d, g, j, m, n], [a, d, g, j, m, o], [a, d, g,j, m, p], [a, d, g, k, l, n], [a, d, g, k, l, o], [a, d, g, k, l, p], [a, d, g, k, m, n], [a, d, g, k, m, o], [a, d, g, km, p], [a, d, h, j, l, n], [a, d, h,j, l, o][a, d, h, j, l, p], [a, d, h, j, m, n], [a, d, h,j, m, o], [a, d, h,j, m, p], [a, d, h, k, l, n], [a, d, h, k, l, o], [a, d, h, k, l, p], [a, d, h, k, m, n], [a, d, h, k, m, o], [a, d, h, k, m, p], [a, d, i, j, l, n], [a, d, i, j, l, o], [a, d, i, j, l, p], [a, d, i, j, m, n], [a, d, i,j, m, o], [a, d, i, j, m, p], [a, d, i, k, l, n], [a, d, i, k, l, o], [a, d, i, k, l,p], [a, d, i, k, m, n], [a, d, i, k, m, o], [a, d, i, k, m, p], [a, e, g, j, l, n], [a, e, g, j, l, p], [a, e, g, j, m, n], [a, e, g, j, m, o], [a, e, g, j, m,o], [a, e, g, j, m, p], [a, e, g, k, l, n], [a, e, g, k, l, o], [a, e, g, k, m, n], [a, e, g, k, m, n], [a, e, g, k, m, o], [a, e, g, k, m, p], [a, e, h, j, l, n], [a, e, h, j, l, o], [a, e, h, j, l,p], [a, e, h,j, m, n], [a, e, h, j, m, o], [a, e, h i, m, p], [a, e, h, k, l, n], [a, e, h, k, l, o], [a, e, , k, l, p], [a, e, h, k, m, n], [a, e, h, k, m, o], [a, e, h, k, p], [a, e, i, j, l, n], [a, e, i, j, l, o], [a, e, i, j, l, p], [a, e, i, j, m, n], [a, e, i, j, m, o], [a, e, i, j, m, p], [a, e, i, k, l, n], [a, e, i, k, l, o], [a, e, i, k, 1 p], [a, e, i, k, m, n], [a, e, i, k, m, o], [a, e, i, k, m, p], [a, f, g, j, l, n], [a, f, g, j, l, o], [a, f, g,j, , p], [a, f g,j, m, n], [a, f, g, j, m, o], [a, f, g, j, m, p], [a, f, g, k, l, n], [a, f, g, k, l, o], [a, f, g, k, l, p], [a, f, g, k, m, n], [a,f, g, k, m, o], [a, f, g, k, m, p], [a, f, h, j, l, n], [a, f, h, j, o], [a, f, h, j, l, p], [a, f, h, j, m, n], [a, f, h, j, m, o], [a, f, h, j, m, p), [a, f, h, k, l, n], [a, f, h, k, l, o], [a, f, h, k, l, p], [a, f, h, k, m, n], [a, f, h, k, o], [a, f, h, k, m, p], [a, f, i, j, l, n], [a, f i, j, l, o], [a, f, i, j, l, p], [a, f, i, j, m, n], [a, f, i, j, m, o], [a, f, i, j, m, p], [a, f i, k, l, n], [a, f, i, k, l, o], [a, f, i, k, l, p], [a, f, i, k, m, n], [a, f, i, k, m, o], [a, f, i, k, n, p], [b, d, g, j, l, n], [b, d, g, j, l, o], [b, d, g, j, l, p], [b, d, g, j, m, n], [b, d, g, j, m, o], [b, d, g, j, m, p], [b, d, g, k, l, n], [b, d, g, k, l, o], [b, d, g, k, l, p], [b, d, g, k, m, n], [b, d, g, k, m o], [b, d, g, k, m, p], [b, d, h, j, l, n], [b, d, h, j, l, o], [b, d, h, j, l, p], [b, d, h, j, m, n], [b, d, h, j, m, o], [b, d, h, j, m, p], [b, d, h, k, l, n], [b, d, h, k, l, o], [b, d, h, k, l, p], [b, d, h, k, m, n], [b, d, h, k, m, o], [b, d, h, k, m, p], [b, d, i, j, l, n ], [b, d, i, j, l, o], [b, d, i, j, l, p], [b, d, i, j, l, n], [b, d, i, j, m, o], [b, d, i, j, m, p], [b, d, i, k, l, n], [b, d, i, k, l, o], [b, d, i, k, l, p], [b, d, i, k, m, n], [b, d, i, k, m, o], [b, d, i, k, m, p], [b, e, g, j, l, n], [b, e, g, j, l, o], [b, e, g, j, l, p], [b, e, g, j, m, n], [b, e, g, j, m, o], [b, e, g, j, m, p], [b, e, g, k, l, n][b, e, g, k, l, o], [b, e, g, k, l, p], [b, e, g, k, m, n], [b, e, g, k, m, o], [b, e, g, k, m, p], [b, e, h, j, l, n], [b, e, h, j, l, o], [b, e, h, j, l, p], [b, e, h, j, m, n], [b, e, h, j, m, o], [b, e, h, j, m, p], [b, e, h, k, l, n], [b, e, h, k, l, o], [b, e, h, k, l, p], [b, e, h, k, m, n], [b, e, h, k, m, o], [b, e, h, k, m, p], [b, e, i, j, l, n], [b, e, i, j, l, o], [b, e, i, j, l, p], [b, e, i, j, m, n], [b, e, i, j, m, o], [b, e, i, j, m, p], [b, e, i, k, l, n], [b, e, i, k, l, o], [b, e, i, k, l, p], [b, e, i, k, m, n], b, e, i, k, m, o], [b, e, i, k, m, p], [b, f, g, j, l, n], [b, f, g, j, l, o], [b, f, g, j, l, p], [b, f, g, m, n], [b, f, g, j, m, o], [b, f, g, j, m, p], [b, f, g, k, l, n], [b, f, g, k, l, o], [b, f, g, k, l, p], [b, f, g, k, m, n], [b, f, g, k, m, o], [b, f, g, k, m, p], [b, f, h, j, l, n], [b, f, h, j, l, o], [b, f, h, j, l, p], [b, f, h, j, m, n], [b, f, h, j, m, o], [b, f, h, j, m, p], [b, f, h, k, l, n], [b, f, h, k, l, o], [b, f, h, k, l, p], [b, f, h, k, m, n], [b, f, h, k, m, o], [b, f, h, k, m, p], [b, f, i, j, l, n], [b, f, i, j, l, o], [b, f, i, j, l, p], [b, f, i, j, m, n,], [b, f, i, j, m, o], [b, f, i, j, m, p], [b, f, i, k, l, n], [b, f, i, k, l, o], [b, f, i, k, l, p], [b, f, i, k, m, n], [b, f, i, k, m, o], [b, f, i, k, m, p], [c, d, g, j, l, n], [c, d, g, j, l, o], [c, d, g, j, l, p], [c, d, g, j, m, n], [c, d, g, j, m, o], [c, d, g, j, m, p], [c, d, g, k, l, n], [c, d, g, k, l, o], [c, d, g, k, l, p], [c, d, g, k, m, n], [c, d, g, k, m, o], [c, d, g, k, m, p], [c, d, h, j, l, n], [c, d, h, j, l, o], [c, d, h, j, l, p], [c, d, h, j, m, n], [c, d, h, j, m, o], [c, d, h, j, m, p], [c, d, h, k, l, n], [c, d, h, k, l, o], [c, d, h, k, l, p], [c, d, h, k, m, n], [c, d, h, k, m, o], [c, d, h, k, m, p], [c, d, i, j, l, n], [c, d, i, j, l, o], [c, d, i, j, l, p], [c, d, i, j, m, n], [c, d, i, j, m, o], [c, d, i, j, m, p], [c, d, i, k, l, n], [c, d, i, k, l, o], [c, d, i, k, l, p], [c, d, i, k, m, n], [c, d, i, k, m, o], [c, d, i, k, m, p], [c, e, g, j, l, n], [c, e, g, j, l, o], [c, e, g, j, l, p], [c, e, g, j, m, n], [c, e, g, j, m, o], [c, e, g, j, m, p], [c, e, g, k, l, n], [c, e, g, k, l, o], [c, e, g, k, l, p], [c, e, g, k, m, n], [c, e, g, k, m o], [c, e, g, k, m, p], [c, e, h, j, l, n], [c, e, h, j, l, o], [c, e, h, j, l, p], [c, e, h, j, m, n], [c, e, h, j, m, o], [c, e, h, j, m, p], [c, e, h, k, l, n], [c, e, h, k, l, o], [c, e, h, k, l ,p], [c, e, h, k, m, n], [c, e, h, k, m, o], [c, e, h, k, m, p], [c, e, i, j, l, n], [c, e, i, j, l, o], [c, e, i, j, l, p], [c, e, i, j, m, n], [c, e, i, j, m, o], [c, e, i, j, m, p], [c, e, i, k, l, n], [c, e, i, k, l, o], [c, e, i, k, l, p], [c, e, i, k, m, n], [c, e, i, k, m, o], [c, e, i, k, m, p], [c, f, g, j, l, n], [c, f, g, j, l, o], [c, f, g, j, l, p], [c, f, g, j, m, n], [c, f, g, j, m, o], [c, f, g, j, m, p], [c, f, g, k, l, n], [c, f, g, k, l, o], [c, f, g, k, l, p], [c, f, g, k, m n], [c, f, g, k, m, o], [c, f, g, k, m, p], [c, f, h, j, l, n], [c, f, h, j, l, o], [c, f, h, j, l, p], [c, f, h, j, m, n], [c, f, h, j, m, o], [c, f, h, j, m, p], [c, f, h, k, l, n], [c, f, h, k, l, o], [c, f, h, k, l, p], [c, f, h, k, m, n], [c, f, h, k, m, o], [c, f, h, k, m, p], [c, f, i, j, l, n], [c, f, i, j, l, o], [c, f, i, j, l, p], [c, f, i, j, m, n], [c, f, i, j, m, o], [c, f, i, j, m, p], [c, f, i, k, l, n], [c, f, i, k, l, o], [c, f, i, k, l, p], [c, f, i, k, m, n], [c, f, i, k, m, o], [c, f, i, k, m, p]

Preferred embodiments of this invention are compounds wherein Z is any one of (q) to (s) and [(R¹, R²), (R³, R⁴), R⁵, R⁶, X, Y] is any one of the above combinations.

In this specification, the compound represented by the formula (I) wherein R¹ is hydrogen atom may be represented as an isomer of the following formula (V):

wherein R², R³, R⁴, R⁵, R⁶, X, Y, and Z are as defined above and R¹ is hydrogen atom.

The compounds represented by the formula (II), (III), and (IV) may be each isomer as well.

The compound represented by the formula (XXV):

wherein one of R¹⁵ and R¹⁶ is —NR¹R² wherein R¹ and R² are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, an optionally substituted non-aromatic heterocyclic group, or acyl, or R¹ and R² together with the adjacent nitrogen atom may form 3- to 6-membered ring, and the other is alkylthio;

or both of R¹⁵ and R¹⁶ are alkylthio;

R⁵ and R⁶ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alknyl, optionally substituted alkyloxy, alkylthio, optionally substituted alkyloxycarbonyl, optionally substituted aryl, optionally substituted heteroaryl, halogen, hydroxy, mercapto, optionally substituted amino, carboxy, cyano, or nitro;

X is —N(R⁷)—, —NH—NH—, —O—, or —S— wherein R⁷ is hydrogen atom or optionally substituted alkyl;

Y is optionally substituted 5-membered non-aromatic heterocycle-diyl or optionally substituted 5-membered heteroaryl-diyl; and

Z is optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted alkenyl;

the prodrugs thereof, or their pharmaceutically acceptable salts, or their solvates are also useful as a pharmaceutical composition, an anti tumor agent, a cytostatic agent, and an inhibitor against a signal derived from Ras oncogene products.

BEST MODE FOR CARRYING OUT THE INVENTION

The compound of the present invention represented by the formula (I) can be synthesized by the well-known method described in the literature of chemistry. A summary of the useful method for synthesis of the compound of the present invention is shown below.

(Synthetic method)

wherein R¹, R², R³, R⁴, R⁵, R⁶, X, Y, and Z are as defined above; R¹³ is hydrogen atom or a protective group of a hydroxy group.

The compound represented by the formula (I) can be synthesized by reacting Z—Y—XH (VI) with the guanidinopyrimidine derivatives (VII). The guanidinopyrimidine derivatives (VII) in a solvent such as water, acetic acid, pyridine, and the like is treated with a hydrohalogenic acid such as hydrochloric acid and hydrobromic acid to give hydrogen halide salts of 5-halogenomethylpyrimidine. When R¹³ is hydrogen atom, a halogenation agent such as thionyl halide and phosphorous halide can be used. The obtained salt and Z—Y—XH (VI) in a solvent such as water, methanol, ethanol, N,N-dimethylformamide, dimethylsulfoxide, tetrahydrofuran are reacted with an appropriate base, for example an inorganic base such as sodium hydroxide, potassium butoxide, sodium hydride, potassium hydride, and potassium carbonate or an organic base such as triethylamine, pyridine, and diisopropylethylamine, at −20° C. to 100° C., preferably 0° C. to 30° C. for 1 min to 24 h, preferably 10 min to 12 h to give the aimed compound (I).

Compound (VI) and compound (VII) can be synthesized by the methods A to I and the methods J to N as shown below.

In the methods A to I, Z represents optionally substituted aryl or optionally substituted heteroaryl. The starting material of each method is commercially available or can be synthesized by well-know method from the compound which is commercially available.

Method A: Synthetic method of the compound wherein Y is an oxadiazole ring and X is —S—.

Compound (VIII) in a solvent such as ethanol and benzene is reacted with carbon disulfide and a base such as triethylamnine, sodium hydroxide, potassium carbonate at 0° C. to 100° C., preferably 60° C. to 100° C. for 10 min to 24 h, preferably 2 h to 12 h to give compound (VI-1).

Method B: Synthetic method of the compound wherein Y is an oxadiazole ring and X is —O—.

To a solution of compound (VIII) in a solvent such as tetrahydrofuran and toluene is added carbonyldiimidazole and the mixture is reacted at 0° C. to 120° C., preferably 60° C. to 120° C. for 10 min to 24 h, preferably 2 h to 12 h to give compound (VI-2).

Method C: Synthetic method of the compound wherein Y is an oxadiazole ring and X is —N(R⁷)—.

wherein R⁷ is as defined above.

To a solution of compound (IX) in a solvent such as ethanol and tetrahydroftiran is added mercury oxide and the mixture is reacted at 0° C. to 120° C., preferably 30° C. to 80° C. for 0.5 h to 24 h, preferably 1 h to 24 h to give compound (VI-3).

Method D: Synthetic method of the compound wherein Y is a thiadiazole ring and X is —S—.

To a solution of compound (VIII) in a solvent such as ethanol and tetrahydrofuran are added carbon disulfide and a base such as triethylamine and sodium hydroxide and the mixture is reacted at 0° C. to 100° C., preferably 20° C. to 60° C. for 0.5 h to 24 h, 1 h to 12 h. After the solvent is removed, the residue is reacted with conc. sulfuric acid at −20° C. to 40° C., preferably 0° C. to 20° C. for 1 min to 12 h, preferably 10 min to 1 h to give compound (VI-4).

Method E: Synthetic method of the compound wherein Y is a furan ring and X is —S—.

(Step 1)

Halogenated furan such as 2-bromofuran is reacted with compound (X) in a solvent such as dimethylformamide, toluene, xylene, benzene, tetrahydrofliran, and ethanol in the presence of palladium catalyst such as Pd(Ph₃P)₄ and a base such as potassium carbonate, calcium carbonate, triethylamine, and sodium methoxide to give the aimed compound (XI) (Suzuki reaction). The reaction temperature is room temperature to 100° C., preferably room temperature to 80° C. and the reaction time is 5 to 50 h, preferably 15 to 30 h.

(Step 2)

To a solution of compound (XI) in a solvent such as tetrahydrofuran, diethyl ether, and toluene is added a base such as n-butyllithium and sec-butyllithium and the mixture is stirred at −100° C. to 50° C., preferably −80° C. to 0° C. for 1 min to 24 h, preferably 10 min to 60 min. To the mixture is added sulfur and the resulting mixture is reacted at −100° C. to 50° C., preferably −80° C. to 0° C. for 1 h to 24 h, preferably 1 h to 12 h to give the a compound (VI-5).

Method F: Synthetic method of the compound wherein Y is a thiophene ring and X is —S—.

wherein Hal is halogen.

The steps 1 and 2 can be carried out in a manner similar to those described in step 1 and 2 of Method E.

Method G: Synthetic method of the compound wherein Y is an oxazole ring and X is —S—.

To a solution of compound (XIII) in a solvent such as dichloromethane, toluene, and diethyl ether is added thiophosgene in the presence of a base such as triethylamine and sodium hydroxide and the mixture is reacted at −20° C. to 100° C., preferably 0° C. to 40° C. for 1 h to 48 h, preferably 1 h to 24 h to give compound (VI-7).

Method H: Synthetic method of the compound wherein Y is an oxazole ring and X is —O— or —S—.

(Step 1)

Compound (XIV) in a solvent such as dichloromethane and acetonitrile is reacted with a condensing agent such as dicyclohexylcarbodiimide at −20° C. to 50° C., preferably 0° C. to 20° C. for 5 min to 24 h, preferably 10 min to 2 h to give compound (VI-8).

(Step 2)

To a solution of compound (VI-8) in a solvent such as toluene and dioxane is added Lawesson's reagent and the mixture is reacted at 60° C. to 150° C., preferably 80° C. to 120° C. for 1 h to 24 h, preferably 2 to 12 h to give compound (VI-9).

Method I: Synthetic method of the compound wherein Y is an isoxazole ring and X is —O— or —S—.

wherein R¹⁴ is C1 to C3 alkyl.

(Step 1)

Compound (XV) in a solvent such as methanol and tetrahydrofuran is reacted with hydroxylamine at 20° C. to 100° C., preferably 50° C. to 80° C. for 1 h to 24 h, preferably 2 h to 12 h to give compound (VI-10).

(Step 2)

Compound (VI-11) can be obtained in a manner similar to that described in step 2 of Method H.

The compounds which are not concretely shown in the above methods can be synthesized by a combination of some of the above methods A to I and well-know method.

In the methods J to N, R¹, R², R³, R⁴, R⁵, R⁶, and R¹³ are as defined above. The starting material of each method is commercially available or can be synthesized by well-know method from the compound which is commercially available.

Methods J and K are process for construction of a pyrimidine ring and can be carried out in accordance with well-known method (see Journal of Chemical Society, 1937, p-364, ibid., 1943, p-388 and J. Pharm. Soc. Japan 1954, p-742).

Methods L to N are processes that a guanidino group is introduced to the pyrimidine derivative obtained in the Method J and Method K and can be carried out in accordance with well-known method (see Journal of Chemical Society, 1948, p-58, ibid., 1946, p-1063 and Synthesis, 1988, p-460).

Method J: Synthesis of a pyrimidine ring

(Step 1)

Compound (XVI) in a solvent such as ethanol, tetrahydrofuran, and dimethylformamide is reacted with R⁵—C(═S)—NH₂ in the presence of a base such as sodium ethylate and sodium hydroxide at 0° C. to 150° C., preferably 60° C. to 100° C. for 0.5 h to 48 h, preferably 1 h to 12 h to give compound (XVII).

(Step 2)

Compound (XVII) in a solvent such as ether and tetrahydrofuran or a mixed in solvent such as ether-tetrahydrofuran is reacted with a reducing agent such as lithium aluminum hydride and lithium borohydride at −80° C. to 100° C., preferably −20° C. to 40° C. for 0.5 h to 24 h, preferably 1 h to 12 h to give an alcohol derivative. The obtained alcohol derivative is protected by the method described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons) and the like to give compound (XVIII). Methyl, ethyl, trimethylsilyl, tert-butyldimetylsilyl, and the like are exemplified as R¹³.

Method K: Synthesis of a pyrimidine ring

(Step 1)

Compound (XIX) in a solvent such as ethanol, tetrahydrofuran, and dimethylformamide is reacted with R⁵—C(═NH)—NH₂ or its salt in the presence of a base such as sodium ethylate and sodium hydroxide at 0° C. to 150° C., preferably 60° C. to 100° C. for 0.5 h to 48 h, preferably 1 h to 12 h to give compound (XX) or its salt.

(Step 2)

Compound (XX) or its salt in a solvent such as toluene and dichloroethane or without a solvent is reacted with a halogenation agent such as thionyl chloride and phosphorus oxychloride at 0° C. to 150° C., preferably 60° C. to 120° C. for 0.5 h to 12 h, preferably 1 h to 5 h to give a halogenated derivative. The obtained halogenated derivative in a solvent such as ethanol and tetrahydrofuran is reacted with R¹NH₂ at −80° C. to 100° C., preferably −20° C. to 30° C. for 0.5 h to 48 h, preferably 1 h to 12 h to give compound (XX).

(Step 3)

This step can be carried out in a manner similar to that described in step 2 of Method J.

Method L: Introduction of a guanidino group

(Step 1)

Compound (XVIII) in a solvent such as dimethylformamide, pyridine, and tetrahydrofuran is reacted with R³-NCS or R³R⁴NCS-Hal wherein Hal is halogen in the presence or absence of a base such as sodium hydride at −20° C. to 120° C., preferably 0° C. to 120° C. for 0.5 h to 48 h, preferably 1 h to 24 h to give compound (XXII).

(Step 2)

To a solution of compound (XXII) in a solvent such as methanol and tetrahydrofiran are added a heavy metal salt or heavy metal oxide such as HgO and R¹R²NH and the mixture is reacted at −20° C. to 100° C., preferably 0° C. to 50° C. for 0.5 h to 48 h, preferably 1 h to 12 h to give compound (VII).

Method M: Introduction of a guanidino group

(Step 1)

Compound (XVIII) in a solvent such as dimethylformamide and tetrahydrofuran is reacted with a base such as sodium hydride and potassium butoxide at 0° C. to 100° C., preferably 20° C. to 60° C. for 0.5 h to 48 h, preferably 1 h to 12 h. To the mixture are added carbon disulfide and then methyl iodide and the resulting mixture is reacted at 0° C. to 100° C., preferably 20° C. to 60° C. for 0.5 h to 48 h, preferably 1 h to 12 h to give compound (XXII).

(Step 2)

Compound (XXIII) in a solvent such as methanol and dimethylformamide is reacted with R³R⁴NH at 0° C. to 150° C., preferably 0° C. to 100° C. for 0.5 h to 48 h, preferably 1 h to 12 h to give compound (XXIV).

(Step 3)

Compound (XXIV) in a solvent such as methanol and dimethylformamide is reacted with R¹R²NH at 20° C. to 150° C., preferably 40° C. to 80° C. for 0.5 h to 48 h, preferably 4 h to 24 h to give compound (VII).

Method N: Introduction of a guanidino group (R¹═H)

(Step 1)

This step can be carried out in a manner similar to that described in step 1 of Method L.

(Step 2)

This step can be carried out in a manner similar to that described in step 2 of Method L.

When a compound contains a functional group(s) possibly interfering the reaction such as hydroxy, mercapto, and amino in the each step of Method A to Method N, it can previously be protected and deprotected at an appropriate stage in accordance with the literature such as Protective Groups in Organic Synthesis, Theodora W. Green (John Wiley & Sons).

In the specification, the term “solvate” includes, for example, solvates with organic solvents, hydrates, and the like.

The term “the compounds of the present invention” herein used includes pharmaceutically acceptable salts and hydrates of the compounds. For example, salts with alkali metals (e.g., lithium, sodium, and potassium), alkaline earth metals (e.g., magnesium and calcium), ammonium, organic bases, amino acids, mineral acids (e.g., hydrochloric acid, hydrobromic acid, phosphoric acid, and sulfuric acid), or organic acids (e.g., acetic acid, citric acid, maleic acid, fumaric acid, benzenesulfonic acid, and p-toluenesulfonic acid) and hydrates of them are exemplified. These salts and hydrates can be formed by usual methods. The hydrates may coordinate with an arbitrary number of water molecules.

Prodrug is a derivative of the compound of the present invention having a group which can be decomposed chemically or metabolically, and such prodrug is converted to a pharmaceutically active compound of the present invention by means of solvolysis or by placing the compound in vivo under a physiological condition. The selection method and the process method of an appropriate prodrug derivative are described in the literature such as Design of Prodrugs, Elsevier, Amsterdam 1985. When the compounds of the present invention have a carboxyl group, an ester derivative prepared by reacting a basal acid compound with a suitable alcohol or an amide prepared by reacting a basal acid compound with a suitable amine are exemplified as prodrugs. Particularly preferred esters as prodrugs are methyl ester, ethyl ester, n-propyl ester, isopropyl ester, n-butyl ester, isobutyl ester, tert-butyl ester, morpholinoethyl ester, N, N-diethylglycolamido ester, and the like. When the compounds of the present invention have a hydroxy group, an acyloxy derivative prepared by reacting with a suitable acyl halide or a suitable acid anhydride are exemplified as prodrugs. Particularly preferred acyloxy derivatives as prodrugs are —OCOC₂H₅, —OCO^(t)—Bu, —OCOC₁₅H₃₁, —OCO(m—COONa—Ph), —OCOCH₂CH₂COONa, —OCOCH(NH₂)CH₃, and —OCOCH₂N(CH₃)₂, and the like. When the compounds of the present invention have an amino group, an amide derivative prepared by reacting with a suitable acid halide or a suitable acid anhydride are exemplified as prodrugs. Particularly preferred amide derivatives as prodrugs are —NHCO(CH₂)₂₀CH₃ and —NHCOCH(NH₂)CH₃, and the like.

The compound of the present invention is not restricted to any particular isomers but includes all possible isomers and racemic modifications.

The compounds of the present invention have an inhibitory activity against a signal derived from Ras oncogene products as shown in the experimental examples below.

Consequently, the compounds of the present invention can be used as a therapeutic agent for cancer.

When the compound of this invention is administered to a patient for the treatment or prevention of the above diseases, it can be administered by oral administration such as powder, granules, tablets, capsules, pilulae, and liquid medicine, or by parenteral administration such as injections, suppository, percutaneous formulations, insufflation, or the like. An effective amount of the compound of tis invention is formulated by being mixed with appropriate medicinal admixture such as excipient, binder, penetrant, disintegrators, lubricant, and the like, if necessary. When parenteral injection is prepared, the compound of this invention and an appropriate carrier are sterilized to prepare it.

An appropriate dosage varies with the conditions of the patients, an administration route, their age, and their body weight. In the case of oral administration to an adult, the dosage can generally be between 0.01-100 mg/kg/day, preferably 0.1-20 mg/kg/day.

The following examples are provided to further illustrate the present invention and are not to be construed as limiting the scope thereof.

In the examples, the following abbreviations are used.

Me: methyl

Et : ethyl

Pr: n-propyl

i-Pr: isopropyl

Bu : n-butyl

i-Bu: isobutyl

tBu: tert-butyl

Ac: acetyl

Ph: phenyl

MPM: p-methoxyphenylmethyl

DMF: dimethylformamide

THF: tetrahydrofuran

DMSO: dimethylsulfoxide

TsOH: p-toluene sulfonic acid

TBS : tert-butyldimethylsilyl

In ¹H-NMR, the value of δ is represented by ppm, s is singlet, d is doublet, t is triplet, q is quartet, quit is quintet, sext is sextet, and br is broad. The value of J is represented by Hz.

EXAMPLE Reference Example 1

Step 1

To a suspension of lithium aluminum hydride (4.4 g) in 220 ml of THF was added dropwise a solution of compound 1 (22.0 g) which was obtained by well-known method (G. W. Kenner, B. Lythgoe, A. R. Todd and A. Topham, J. Chem. Soc., 388(1943)) in 220 ml of THF with stirring at ice-cooling. The reaction mixture was allowed to room temperature and stirred for 2 h. To the resulting mixture was added excess ice and stirred for an additional 2 h. Anhydrous sodium sulfate was added to the mixture and the precipitate was filtered off and washed with methanol. The combined filtrate was concentrated in vacuo and the residue was dissolved in ethanol with heating. The appeared insoluble material was filtered off and ethanol solution was allowed to cool. The insoluble material was filtered off again. The filtrate was diluted with diethyl ether and appeared crystal was filtered to give 14.5 g of compound 2.

Melting point: 119-121° C.; ¹H-NMR(CDCl₃): 0.09(6H, s), 0.90(9H, s), 2.50(3H, s), 4.60(2H, s), 5.39(2H, br), 7.95(1H, s).

Step 2

To a solution of compound 2 (13.9 g) and 7.7g of imidazole in 200 ml of DMF was added 7.7 g of t-butyldimethylsilyl chloride with stirring at ice-cooling. The mixture was stirred over night and 2.0 g of imidazole and 3.4 g of t-butyldimethylsilyl chloride were added to the mixture. The mixture was stirred for 6 h and added ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. Ethyl acetate was added to the residue and the mixture was diluted with hexane. The appeared crystal was filtered to give 12.8 g of compound 3.

Melting point: 119-121° C.; ¹H-NMR(CDCl₃): 0.09(6H, s), 0.90(9H, s), 2.50(3H, s), 4.60(2h, s), 5.39(2H, br), 7.95(1H, s).

Step 3

To a suspension of 2.9 g of sodium hydride in 90 ml of DMF was added dropwise a solution of compound 3 (18.1 g) in 90 ml of DMF with stirring. The mixture was stirred for lh and 6.3 ml of ethyl isothiocyanate was added to the mixture dropwise at ice-cooling. The resulting mixture was stirred for an additional 30 min at room temperature, ice-cooled, added 4.5 ml of acetic acid, and added ethyl acetate. The organic layer was washed with aqueous potassium hydrogen sulfate and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was subjected to silica gel column chromatography to give 15.8 g of compound 4.

Melting point: 86-87° C.; ¹H-NMR(CDCl₃): 0.17(6H, s), 0.95(9H, s), 1.36(3H, t, J=7.3 Hz), 2.60(3H, s), 3.76(2H, dq, J=4.9, 7.3 Hz), 4.69(2H, s), 8.19(1H, s), 9.36(1H, br), 11.5(1H, br).

Step 4

To the mixture of compound 4 (8.0 g), 5.6 g of mercuric oxide (red), and 60 ml of methanol was added 40 % methylamine in methanol with stirring at room temperature. The resulting mixture was stirred for 4h and insoluble material was filtered off. The filtrate was concentrated in vacuo and methanol/diethyl ether was added to the residue. The insoluble material was filtered off and the solvent was concentrated in vacuo. Toluene/hexane was added to the residue to give 7.81 g of compound 5 as crystal.

Melting point: 150-151° C.; ¹H-NMR(CDCl₃): 0.10(6H, s), 0.95(9H, s), 1.28(3H, t, J=7.0 Hz), 2.49(3H, s), 2.92(3H, d, J=4.9 Hz), 3.34(2H, quint, J=7.0 Hz), 4.76(2H, s), 8.30(1H, s).

Reference Example 2

Step 1

To a solution of phosphorus oxychloride (61.5 g) in 35 ml of toluene was added 9.0 g of a sodium salt of compound 6 which was obtained by well-known method (A. Kreutzberger and C. Grundmann, J. Org. Chem., 26, 388 (1961)) and the resulting mixture was stirred for 1 h at 100° C. Excess phosphorus oxychlorde was removed under reduced pressure and 18 ml of 10% ammonia in ethanol was added to the mixture at 0° C. The mixture was stirred for 130 min at room temperature and insoluble material was removed. The solvent was concentrated in vacuo and the resulting residue was purified by column chromatography on silica gel to give 4.78 g of compound 7.

¹H-NMR(CDCl₃): 1.40(3H, t, J=7.3 Hz), 4.38(2H, q, J=7.3 Hz), 5.61(1H br), 7.86(1H, br), 8.62(1H, s), 8.90(1H, s).

Step 2

To a suspension of lithium aluminum hydride (1.19 g) in 30 ml of THF was added a solution of compound 7 (4.77 g) in 42 ml of THF at 0° C. and the resulting mixture was stirred for 1 h. A little water was added to the mixture and then stirred for an additional 50 min. The insoluble material was filtered off and the filtrate was concentrated in vacuo. Recrystallization from ethanol gave 1.77 g of compound 8.

¹H-NMR(CDCl₃): 4.65(2H, s), 8.09(1H, s), 8.54(1H, s).

Step 3

To a solution of compound 8 (1.63 g) in 13 ml of DMF was added a solution of 1.33 g of imidazole and 2.36 g of t-butyl dimethylsilyl chloride in 13 ml of DMF and the resulting mixture was stirred for 19 h at room temperature. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried, and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give 2.68 g of compound 9.

¹H-NMR(CDCl₃): 0.10(6H, s), 0.90(9H, s), 4.62(2H, s), 5.43(2H, br), 8.04(1H, s), 8.51(1H, s).

Step 4

To a suspension of 1.67 g of sodium hydride in 10 ml of DMF was added a solution of compound 9 (4.00 g) and 3. 81 g of carbon disulfide in 40 ml of DMF. After stirring for 1 h at room temperature, to the mixture was added 7.11 g of methyl iodide and resulting mixture was stirred for an additional 4 h. To the mixture was added aqueous potassium hydrogen sulfate and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried, and concentrated in vacuo. To the residue was added 70% ethtylamine solution (21.4 g) and the mixture was stirred for 15 h at 60° C. Excess ethylamine was removed under reduced pressure. The resulting residue was purified by column chromatography on silica gel to give 3.11 g of compound 10.

¹H-NMR(CDCl₃): 0.11(6H, s), 0.96(9H, s), 1.28(6H, t, J=7.3 Hz), 3.33(4H, dq, J=5.6, 7.3Hz), 4.77(2H, s), 8.38(1H, s), 8.52(1H, s).

Reference Example 3 Synthesis of Compound G-1

Step 1

To a solution of 4-amino-5-ethoxymethyl-2-methylpyrimidine 11 (1.0 g) which was obtained by well-known method (M. Tomita, S. Uyeo, A. Takamizawa, and R. Maeda, Yakugakuzassi, 74, 742 (1943)) and 0.74 g of potassium t-butoxide in 12 ml of DMF was added dropwise 0.58 ml of ethyl isothiocyanate with stirring at ice-cooling. After the addition was completed, the mixture was stirred for 1 h at room temperature. The disappearance of compound 11 was confirmed, then to the mixture was added 0.42 ml of methyl iodide at ice-cooling and the resulting mixture was stirred for 10 min at ice-cooling and for an additional 10 min at room temperature. The reaction mixture was extracted with ethyl acetate and the organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was subjected to silica gel column chromatography to yield 1.42 g of compound 12.

Melting point 52-53° C.; ¹H-NMR(CDCl₃): 1.26(3H, t, J=6.9 Hz), 1.33(3H, t, J=7.3 Hz), 2.51(3H, s), 2.55(3H, s), 3.43(2H, dq, J=7.3, 5.3 Hz), 3.60(2H, q, J=6.9 Hz), 4.61(2H, s), 8.41(1H, s), 11.18(1H, br).

Step 2

Compound 12 was dissolved in 25 % solution of hydrogen bromide in acetic acid (35 ml) and the mixture was stirred for 8 h at 70° C. The solvent was removed under reduced pressure. The residue was dissolved in 15 ml of DMF and the resulting mixture was added to a suspension of 2-(4-nitrophenyl)-5-mercapto-1,3,4-oxadiazole (2.69 g) and potassium carbonate (6.05 g) in 15 ml of DMF. After the reaction mixture was stirred for 1.5 h at room temperature, water was added to the mixture. The precipitated crystal was collected by filtration to give 4.15 g of compound G-1.

Melting point 156-157° C.; ¹H-NMR(CDCl₃): 1.35(3H, t, J=7.3 Hz), 2.55(3H, s), 2.57(3H, s), 3.45(2H, dq, J=7.3, 5.3Hz), 4.58(2H, s), 8.16(2H, d, J=8.7 Hz), 8.36(2H, d, J=8.7 Hz), 8.53(1H, s), 11.13(1H, br).

Example 1 Synthesis of Compound A-1

Compound 5 (6.5 g) was dissolved in 25% solution of hydrogen bromide in acetic acid and the mixture was stirred over night at 40° C. The solvent was removed under reduced pressure and the residue was dissolved in 43 ml of methanol. The mixture was added to a solution of 2-(2-aminophenyl)-5-mercapto-1,3,4-oxadiazole (11.9 g) which was obtained in accordance with the method described in R. W. Young and K. H. Wood, J. Am. Chem. Soc., 77, 400 (1955) and potassium hydroxide (3.3 g) in 54.5 ml of methanol at ice-cooling. The reaction mixture was stirred for 3 h at room temperature and insoluble material was removed by filtration. The solvent was removed under reduced pressure. To the residue was added dichloromethane and precipitate was removed by filtration. The solvent was removed under reduced pressure and the residue was subjected to silica gel column chromatography to give compound A-1. Further purification by the crystallization from diethyl ether gave 5.6 g of compound A-1. The physical data was shown in Table 1.

Example 2 Synthesis of Compound A-2

To a solution of compound A-1 (4.77 g) in 120 ml of pyridine was added dropwise 1.0 ml of acetyl chloride with stirring at ice-cooling. After 2.5 h, the mixture was warmed to room temperature and stirred for an additional 30 min. To the mixture was added about 5% of methanol in chloroform. The organic layer was washed with sat. sodium bicarbonate aq., dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give 4.37 g of compound A-2. The physical data was shown in Table 1.

Example 3 Synthesis of Compound A-3

Compound 10 (0.17 g) was dissolved in 25% solution of hydrogen bromide in acetic acid (1 ml) and the mixture was stirred for 15 h at 40° C. The solvent was removed under reduced pressure and the residue was dissolved in 3 ml of DMF. The mixture was added to a solution of 2-(4-aminophenyl)-5-mercapto-1,3,4-oxadiazole (0.12 g) and potassium t-butoxide (0.2 g) in 1 ml of DMF at ice-cooling. The reaction mixture was stirred for 1 h at room temperature and extracted with ethyl acetate. The organic layer was washed with water and dried. The residue was purified by silica gel column chromatography to give 0.07 g of compound A-3. The physical data was shown in Table 1.

Example 4 Synthesis of Compound A-4

To a solution of 4-amino-5-ethoxymethyl-2-methylpyridine (4.8 g) which was obtained in accordance with the method described in M. Tomita, S. Uyeo, A. Takamizawa and R. Maeda, Yakugakuzasshi, 74, 742 (1954) in 48 ml of pyridine was added 4.2 g of methyl isothiocyanate and the resulting mixture was heated at reflux for 7 h. Additionally, 1.1 g of methyl isothiocyanate was added and the mixture was heated at reflux for 4 h. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography to give 4.18 g of 4-(N′-methylthioureido)-5-ethoxymethyl-2-methylpyrimidine.

¹H-NMR (CDCl₃): 1.35(3H, t, J=7.0 Hz), 2.61(3H, s), 3.28(3H, d, J=4.9 Hz), 3.62(2H, q, J=7.0 Hz), 4.52(2H, s), 8.23(1H, s), 9.48(1H, br), 11.40(1H, br).

To a solution of 4-(N′-methylthioureido)-5-ethoxymethyl-2-methylpyrimidine(300 mg) in 6 ml of 10% ammonia—ethanol was added 400 mg of red mercuric oxide and the resulting mixture was stirred for 15 min at room temperature. After removing the insoluble material by filtration, crystallization from ethyl acetate gave 117 mg of 4-(methylguanidino)-5-ethoxymethyl−2-methylpyrimidine.

¹H-NMR (CDCl₃): 1.26(3H, t, J=7.0 Hz), 2.51(3H, s), 2.92(3H, s), 3.59(2H q, J=7.0 Hz), 4.52(2H, s), 6.49(1H, s), 8.25(1H, s).

A solution of 4-(methylguanidino)-5-ethoxymethyl-2-methylpyrimidine (500 mg) in 10 ml of 25% of hydrogen bromide in acetic acid was heated at reflux for 6 h. The solvent was removed under reduced pressure and the residue was dissolved in 14.5 ml of ethanol. To the mixture were added 2-(2-aminophenyl)-5-mercaptooxadiazole (290 mg) and potassium hydroxide (350 mg) and the resulting mixture was stirred for 2 h at ice-cooling. The insoluble material was removed by filtration and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography to give 210 mg of the desired compound. The physical data was shown in Table 1.

Example 5 Synthesis of Compound A-5

To a suspension of compound A-4 (200 mg) in 5 ml of methanol was added 5 ml of 10% hydrochloric acid in methanol and the resulting mixture was stirred for 5 min. The solvent was removed under reduced pressure and the residue was dissolved in ethanol. To the solution was added ethyl acetate and the precipitate was collected to give 193 mg of compound A-5.

The result of elemental analysis (C, H, N, Cl) showed the compound was dihydrochloride. The physical data was shown in Table 1.

Example 6-Example 190

Compounds A-6 to A-190 were synthesized in a manner similar to those described in Example 1 to 5. The physical data were shown in Tables 1 to 21. CDCl₃ was used when there is no description of the solvents for the ¹H-NMR spectrum.

TABLE 1

or

Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ Salt ¹H-NMR (δ) ppm 1 A-1 Et Me Me 2-NH₂ — 2.48(3H, s), 4.46(2H, s), 4.54(2H, s), 5.75(2H, br), 6.72(1H, ddd, J= 8.1, 7.2, 0.9), 6.76(1H, dd, J=8.5, 0.9), 7.24(1H, ddd, J=8.5, 7.2, 1.5), 7.27-7.39(5H, m), 7.63(1H, dd, J=8.1, 1.5), 8.40(1H, s) 2 A-2 Et Me Me 2-NHAc — 1.31(3H, t, J=7.2), 2.31(3H, s), 2.49(3H, s), 2.98(3H, d, J=4.9), 3.41(2H, br.), 4.50(2H, s), 7.14(1H, t, J=8.1), 7.49(1H, ddd, J=8.5, 8.1, 1.6), 7.80(1H, dd, J= 8.1, 1.6), 8.35(1H, s), 8.76(1H, d, J=8.5), 10.84(1H, br) 3 A-3 Et Et H 4-NH₂ — 1.30(6H, t, J=7.3), 3.38(4H, br), 4.01(2H, s), 4.45(2H, s), 6.71(2H, d, J=8.5), 7.77(2H, d, J=8.5), 8.39(1H, s), 8.54(1H, s) 4 A-4 H Me Me 2-NH₂ — 2.50(3H, s), 2.93(3H, s), 4.44(2H, s), 5.76(2H, br), 6.73(1H, t, J= 7.8), 6.77(1H, d, J=7.8), 7.24(1H, t, J=7.8), 7.64(1H, d, J=7.8), 8.34(1H, s) 5 A-5 H Me Me 2-NH₂ 2HCl 2.60(3H, s), 2.93(3H, s), 4.47(2H, s), 6.98(1H, t, J=7.9), 7.07(1H, d, J=7.9), 7.45(1H, t, J=7.9), 7.67(1H, d, J=7.9), 8.48(1H, s) (in D₂O) 6 A-6 H Me Me 2-NH₂ TsOH 2.39(3H, s), 2.52(3H, s), 2.86(3H, s), 4.39(2H, s), 6.90(1H, t, J= 7.8), 7.00(1H, d, J=7.8), 7.35(2H, t, J=8.4), 7.41(1H, t, J=7.8), 7.64(1H, d, J=7.8), 7.69(2H, d, J= 8.4), 8.29(1H, s) (in D₂O) 7 A-7 H Me Me 2-NH₂, 5-Cl — 2.51(3H, s), 2.94(3H, s), 4.46(2H, s), 5.79(2H, br), 6.71(1H, d, J= 8.7), 7.18(1H, dd, J=8.7, 2.5), 7.60(1H, d, J=2.5), 8.34(1H, s) 8 A-8 H Et Me 2-NH₂ — 1.31(3H, t, J=7.3), 2.51(3H, s), 3.33(2H, br), 4.47(2H, s), 5.76(2H, br), 6.72(1H, t, J=7.8), 6.77(1H, d, J=7.8), 7.24(1H, t, J= 7.8), 7.64(1H, d, J=7.8), 8.38(1H, s)

TABLE 2 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ Salt ¹H-NMR (δ) ppm 9 A-9 H Bu Me 2-NH₂ — 0.98(3H, t, J=7.3), 1.46(2H, sext, J=7.3), 1.65(2H, quint, J=7.3), 2.50(3H, s), 3.25(2H, br), 4.45(2H, s), 5.76(2H, br), 6.73(1H, ddd, J=7.9 7.0, 0.9), 6.77(1H, dd J=8.4, 0.9), 7.24(1H, ddd, J=8.4, 7.0, 1.5), 7.64(1H, dd, J=7.9, 1.5), 8.35(1H, s) 10 A-10 H Et Me 2-NH₂ 2HCl 1.25(3H, t, J=7.3), 2.58(3H, s), 3.26(2H, q, J=7.3), 4.44(2H, s), 6.96(1H, t, J=7.9), 7.05(1H, d, J= 7.9), 7.44(1H, t, J=7.9), 7.66(1H, d, J=7.9), 8.45(1H, s) (in D₂O) 11 A-11 H 4-Cl—C₆H₄ Me 2-NH₂ — 2.53(3H, s), 4.49(2H, s), 5.76(2H, br), 6.73(1H, ddd, J=8.0, 7.0, 0.7), 6.77(1H, dd, J=8.3, 0.7), 7.22-7.26(3H, m), 7.39(2H, d, J= 8.6), 7.65(1H, dd, J=8.0, 1.5), 8.44(1H, s) 12 A-12 H CH₂Ph Me 2-NH₂ — 2.48(3H, s), 4.46(2H, s), 4.54(2H, s), 5.75(2H, br), 6.72(1H, ddd, J= 8.1, 7.2, 0.9), 6.76(1H, dd, J=8.5, 0.9), 7.24(1H, ddd, J=8.5, 7.2, 1.5), 7.27-7.39(5H, m), 7.63(1H, dd, J=8.1, 1.5), 8.40(1H, s) 13 A-13 Et 1- Me 2-NH₂ — 1.21(3H, t, J=7.2), 2.00(4H, br), pyrrolidinyl 2.53(3H, s), 3.27(2H, dq, J=5.6, 7.2), 3.50(4H, br), 4.30(2H, s), 5.79(2H, br), 6.73(1H, dd, J=8.0, 7.1), 6.79(1H, d, J=8.3), 7.25(1H, ddd, J=8.3, 7.1, 1.5), 7.64(1H, dd, J=8.0, 1.5), 7.98(1H, s) 14 A-14 H Et Me 2- — 1.30(3H, t, J=7.3), 2.51(3H, s), NHSO₂ 3.30(2H, br), 3.78(3H, s), (4- 4.46(2H, s), 6.83(2H, d, J=9.0), MeOC₆H₄) 7.10(1H, t, J=7.8), 7.41(1H, t, J= 7.8), 7.67(1H, d, J=7.8), 7.77- 7.81(3H, m), 8.37(1H, s), 10.41(1H, br) 15 A-15 Et Ac Me 2-NH₂ — 1.28(3H, t, J=7.2), 2.23(3H, s), 2.55(3H, s), 3.55(2H, dq, J=5.6, 7.2), 4.48(2H, s), 5.76(2H, br), 6.72(1H, t, J=7.9), 6.77(1H, d, J= 7.9), 7.24(1H, dt, J=1.5, 7.9), 7.63(1H, dd, J=7.9, 1.5), 8.48(1H, s), 8.84(1H, br), 14.12(1H, br)

TABLE 3 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 16 A-16 Et Ac Me 2-NHAc 1.29(3H, t, J=7.3), 2.24(3H, s), 2.32(3H, s), 2.56(3H, s), 3.57(2H, dq, J= 5.6, 7.3), 4.50(2H, s), 7.14(1H, ddd, J= 8.1, 7.1, 1.1), 7.50(1H, ddd, J=8.6, 7.1, 1.5), 7.80(1H, dd, J=8.1, 1.5), 8.51(1H, s), 8.76(1H, dd, J=8.6, 1.1), 8.88(1H, br), 10.80(1H, br), 14.11(1H, br) 17 A-17 H Et Me 2-NHCOPh 1.28(3H, t, J=7.2), 2.50(3H, s), 3.29(2H, q, J=7.2), 4.48(2H, s), 7.20(1H, t, J=7.9), 7.55-7.59(4H, m), 7.86(1H, dd, J=7.9, 1.5), 8.16-8.18 (2H, m), 9.00(1H, d, J=7.9), 11.68(1H, br) 18 A-18 H Et Me 2-NHAc 1.31(3H, t, J=7.2), 2.31(3H, s), 2.51(3H, s), 3.26(2H, q, J=7.2), 4.48(2H, s), 7.14(1H, dd, J=8.0, 7.5), 7.50(1H, ddd, J=8.6, 7.5, 1.5), 7.80(1H, dd J=8.0, 1.5), 8.39(1H, s), 8.76(1H, d, J=8.6), 10.84(1H, br) 19 A-19 H Me Me 2-NHAc 2.31(3H, s), 2.51(3H, s), 2.95(3H, s), 4.48(2H, s), 7.14(1H, t, J=7.8), 7.50(1H, ddd, J=8.5, 7.8, 1.5), 7.79(1H, dd J=7.8, 1.5), 8.39(1H, s), 8.76(1H, d, J=8.5), 10.84(1H, br) 20 A-20 H Me Me 2-NHCOEt 1.31(3H, t, J=7.6), 2.51(3H, s), 2.57(2H, q, J=7.6), 2.95(3H, s), 4.52(2H, s), 7.13(1H, dd, J=7.9, 7.1), 7.49(1H, ddd, J=8.7, 7.1, 1.7), 7.78(1H, dd, J=7.9, 1.7), 8.42(1H, s), 8.77(1H, d, J=8.7), 10.82(1H, br) 21 A-21 Et Me Me H 1.30(3H, t, J=7.2), 2.49(3H, s), 2.97(3H, br), 3.40(2H, br), 4.49(2H, s), 7.45-7.51(3H, m), 7.97-7.99(2H, m), 8.36(1H, s) 22 A-22 H Et Me 2-NHCOEt 1.31(3H, t, J=7.2), 1.32(3H, t, J= 7.6), 2.51(3H, s), 2.56(2H, q, J=7.6), 3.31(2H, q, J=7.2), 4.48(2H, s), 7.14(1H, t, J=7.9), 7.50(1H, dt, J= 1.6, 7.9), 7.80(1H, dd, J=7.9, 1.6), 8.39(1H, s), 8.79(1H, d, J=7.9), 10.83(1H, br) 23 A-23 Et Me Me 2-NHCOEt 1.31(3H, t, J=7.1), 1.32(3H, t, J= 7.6), 2.49(3H, s), 2.56(2H, q, J=7.6), 2.98(3H, d, J=4.7), 3.40(2H, br), 4.50(2H, s), 7.13(1H, t, J=7.8), 7.49(1H, t, J=7.8), 7.80(1H, d, J= 7.8), 8.35(1H, s), 8.79(1H, d, J=7.8)

TABLE 4 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 24 A-24 Et Et Me 2-NH₂ 1.30(6H, t, J=7.2), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 5.76(2H, br), 6.72(1H, dd, J=8.1, 7.1), 6.77(1H, d, J=8.5), 7.24(1H, ddd, J=8.5, 7.1, 1.5), 7.64(1H, dd, J=8.1, 1.5), 8.33(1H, s) 25 A-25 Et Et Me 2-NHAc 1.31(6H, t, J=7.2), 2.31(3H, s), 2.48(3H, s), 3.38(4H, br), 4.49(2H, s), 7.14(1H, ddd, J=8.1, 7.1, 1.0), 7.49(1H, ddd, J=8.5, 7.1, 1.7), 7.80(1H, dd, J=8.1, 1.7), 8.35(1H, s), 8.76(1H, dd, J=8.5, 1.0), 10.8(1H, br) 26 A-26 Et Et Me 2-NHCOEt 1.31(6H, t, J=7.2), 1.32(3H, t, J= 7.6), 2.48(3H, s), 2.57(2H, q, J=7.6), 3.38(4H, br), 4.49(2H, s), 7.13(1H, ddd, J=8.1, 7.1, 1.0), 7.49(1H, ddd, J= 8.5, 7.1, 1.5), 7.80(1H, dd, J=8.1, 1.5), 8.35(1H, s), 8.79(1H, dd, J=8.5, 1.0), 10.8(1H, br) 27 A-27 Et Me Me 2-OH 1.30(3H, t, J=7.2), 2.49(3H, s), 2.97(3H, d, J=4.6), 3.39(2H, br), 4.49(2H, s), 6.97(1H, ddd, J=7.8, 7.1, 1.2), 7.10(1H, dd, J=8.5, 1.2), 7.41(1H, ddd, J=8.5, 7.1, 1.7), 7.65(1H, dd, J=7.8, 1.7), 8.33(1H, s), 9.95(1H, s) 28 A-28 Et Me Me 2- 1.26(3H, t, J=7.2), 1.30(3H, t, J= OCH₂CO₂Et 7.2), 2.48(3H, s), 2.97(3H, t, J=4.4), 3.40(2H, br), 4.25(2H, q, J=7.2), 4.49(2H, s), 4.77(2H, s), 6.92(1H, d, J= 8.3), 7.10(1H, t, J=7.7), 7.45(1H, ddd, J=8.3, 7.7, 1.7), 7.92(1H, dd, J= 7.7, 1.7), 8.33(1H, s) 29 A-29 Et Me Me 2-NHSO₂Me 1.30(3H, t, J=7.2), 2.49(3H, s), 2.97(3H, d, J=4.6), 3.07(3H, s), 3.40(2H, br), 4.49(2H, s), 7.20(1H, t, J=7.9), 7.51(1H, td, J=7.9, 1.5), 7.83(1H, dd, J=7.9, 1.5), 7.85(1H, d, J=7.9), 8.33(1H, s) 30 A-30 —CH₂—CH₂— Me 2-NH₂ 2.52(3H, s), 3.68(4H, s), 4.43(2H, s), 5.76(2H, br), 6.73(1H, t, J=7.8), 6.77(1H, d, J=7.8), 7.24(1H, t, J= 7.8), 7.64(1H, d, J=7.8), 8.36(1H, s) 31 A-31 Et Me Me 2- 1.19(3H, t, J=7.1), 2.53(3H, s), OCH₂CO₂H 2.97(3H, br), 3.45(2H, br), 4.75(2H, s), 5.16(2H, s), 7.03(1H, t, J=7.6), 7.29(1H, d, J=8.4), 7.42(1H, dd, J= 8.4, 7.6), 8.05(1H, d, J=7.6), 8.73(1H, s) (in C₅D₅N)

TABLE 5 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 32 A-32 Et Et Ph 2-NH₂ 1.36(6H, t, J=7.3), 3.42(4H, br), 4.55(2H, s), 5.77(2H, br), 6.72(1H, t, J= 7.9), 6.77(1H, d, J=7.9), 7.24(1H, t, J=7.9), 7.43-7.46(3H, m), 7.65(1H, dd, J=7.9, 1.4), 8.18-8.20(2H, m), 8.53(1H, s) 33 A-33 Et Et H 2-NH₂ 1.31(6H, t, J=7.2), 3.39(4H, br), 4.48(2H, s), 5.77(2H, br), 6.72(1H, dd, J=8.3, 7.8), 6.78(1H, d, J=8.3), 7.24(1H, m), 7.65(1H, d, J=7.8), 8.41(1H, s), 8.55(1H, s) 34 A-34 Et Et SMe 2-NH₂ 1.29(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.44(2H, s), 5.77(2H, br), 6.69-6.79(2H, m), 7.23(1H, d, J= 8.0), 7.65(1H, dd, J=8.0, 1.5), 8.24(1H, s) 35 A-35 Et Et OH 2-NH₂ 1.30(6H, t, J=7.1), 3.39(4H, br), 4.30(2H, s), 5.74(2H, br), 6.73(1H, ddd, J=8.3, 8.1, 1.0), 6.77(1H, d, J= 8.3), 7.25(1H, td, J=8.1, 1.0), 7.57(1H, s), 7.64(1H, dd, J=8.1, 1.5), 8.84(1H, br) 36 A-36 Et Pr Me 2-NH₂ 1.04(3H, t, J=7.3), 1.30(3H, t, J= 7.2), 1.71(2H, sext, J=7.3), 3.28(2H, br), 3.41(4H, br), 4.46(2H, s), 5.76(2H, br), 6.72(1H, ddd, J=8.1, 7.1, 0.9), 6.77(1H, dd, J=8.4, 0.9), 7.24(1H, ddd, J=8.4, 7.1, 1.7), 7.65(1H, dd, J= 8.1, 1.7), 8.32(1H, s) 37 A-37 Et Et Et 2-NH₂ 1.29(6H, t, J=7.5), 1.30(3H, t, J= 7.4), 2.78(2H, q, J=7.4), 3.37(4H, br), 4.47(2H, s), 5.77(2H, br), 6.73- 6.77(2H, m), 7.24(1H, t, J=8.1), 7.64(1H, dd, J=8.1, 1.5), 8.35(1H, s) 38 A-38 Et Me Me 2-NHMe 1.30(3H, t, J=7.2), 2.48(3H, s), 2.97(3H, d, J=4.6), 2.99(3H, d, J= 4.9), 3.39(2H, br), 4.47(2H, s), 6.68(1H, t, J=8.1), 6.74(1H, d, J= 8.5), 7.35(1H, ddd, J=8.5, 8.1, 1.6), 7.36(1H, br), 7.67(1H, dd, J=8.1, 1.6), 8.32(1H, s) 39 A-39 Et Me Me 2-NMe₂ 1.30(3H, t, J=7.2), 2.49(3H, s), 2.76(6H, s), 2.97(3H, d, J=4.9), 3.40(2H, br), 4.47(2H, s), 6.97(1H, t, J= 7.7), 7.06(1H, d, J=8.3), 7.40(1H, ddd, J=8.3, 7.7, 1.7), 7.72(1H, dd, J= 7.7, 1.7), 8.33(1H, s)

TABLE 6 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 40 A-40 Et Me Me 2-NHEt 1.30(3H, t, J=7.1), 1.37(3H, t, J= 7.1), 2.49(3H, s), 2.98(3H, br), 3.32(2H, dq, J=5.1, 7.1), 3.40(2H, br), 4.47(2H, s), 6.66(1H, t, J=7.4), 6.75(1H, d, J=8.7), 7.32(1H, ddd, J= 8.7, 7.4, 1.7), 7.33(1H, br), 7.67(1H, dd, J=7.4, 1.7), 8.33(1H, s) 41 A-41 Et Et Me 3-NH₂ 1.30(6H, t, J=7.2), 2.48(3H, s), 3.37(4H, br), 3.83(2H, br), 4.46(2H, s), 6.80(1H, ddd, J=8.1, 2.4, 1.0), 7.22- 7.35(3H, m), 8.32(1H, s) 42 A-42 Et Et Me 4-NH₂ 1.29(6H, t, J=7.2), 2.48(3H, s), 3.37(4H, br), 4.00(2H, br), 4.38(2H, s), 6.71(2H, d, J=8.5), 7.76(2H, d, J= 8.5), 8.30(1H, s) 43 A-43 Et Et Me 2-NH₂-3-Cl 1.30(6H, t, J=7.3), 2.48(3H, s), 3.37(4H, br), 4.47(2H, s), 6.31(2H, br), 6.67(1H, t, J=6.9), 7.36(1H, dd, J= 6.9, 1.5), 7.59(1H, dd, J=6.9, 1.5), 8.33(1H, s) 44 A-44 Et Et Me 2-NH₂-4-Cl 1.30(6H, t, J=7.3), 2.48(3H, s), 3.37(4H, br), 4.46(2H, s), 5.88(2H, s), 6.69(1H, dd, J=7.6, 1.8), 6.77(1H, d, J=1.8), 7.56(1H, d, J=7.6), 8.31(1H, s) 45 A-45 Et Et Me 2-NH₂-6-Cl 1.30(6H, t, J=7.2), 2.48(3H, s), 3.39(4H, br), 4.67(2H, s), 5.62(2H, br), 6.67(1H, dd, J=8.1, 1.0), 6.79(1H, dd, J=8.1, 1.0), 7.11(1H, t, J=8.1), 8.23(1H, s) 46 A-46 Et Et CF₃ 2-NH₂ 1.32(6H, t, J=7.2), 3.39(4H, br), 4.48(2H, s), 5.76(2H, br), 6.70(1H, ddd, J=8.5, 7.8, 1.0), 6.77(1H, dd, J= 8.3, 1.0), 7.24(1H, ddd, J=8.5, 8.3, 1.5), 7.63(1H, dd, J=7.8, 1.5), 8.50(1H, s) 47 A-47 Et Et Me 2-NH₂-5-Cl 1.30(6H, t, J=7.2), 2.48(3H, s), 3.37(4H, br), 4.47(2H, s), 5.80(2H, br), 6.71(1H, d, J=8.8), 7.18(1H, dd, J= 8.8, 2.4), 7.60(1H, d, J=2.4), 8.31(1H, s) 48 A-48 Et Et CF₃ 2-NHAc 1.32(6H, t, J=7.2), 2.32(3H, s), 3.39(4H, br), 4.50(2H, s), 7.14(1H, ddd, J=8.0, 7.8, 1.0), 7.50(1H, ddd, J= 8.5, 8.0, 1.5), 7.79(1H, dd, J=7.8, 1.5), 8.54(1H, s), 8.76(1H, dd, J=8.5, 1.0), 10.81(1H, s) 49 A-49 Et Et Me 2-NH₂-4-F 1.30(6H, t, J=7.3), 2.47(3H, s), 3.37(4H, br), 4.45(2H, s), 5.93(2H, br), 6.43(1H, m), 6.47(1H, s), 7.62(1H, dd, J=9.8, 6.1), 8.31(1H, s)

TABLE 7 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 50 A-50 Et Et Me 2-NH₂-5-F 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 5.63(2H, br), 6.72(1H, dd, J=9.2, 4.3), 6.99(1H, m), 7.33(1H, dd, J=9.2, 3.1), 8.32(1H, s) 51 A-51 Et Et Me 2-NH₂-6-F 1.31(6H, t, J=7.3), 2.47(3H, s), 3.40(4H, br), 4.45(2H, s), 6.01(2H, br), 6.04-6.56(2H, m), 7.16(1H, dt, J= 7.9, 6.1), 8.33(1H, s) 52 A-52 Et Et Me 2-NH₂-4,5-F₂ 1.31(6H, t, J=7.3), 2.48(3H, s), 3.40(4H, br), 4.46(2H, s), 5.78(2H, br), 6.55(1H, dd, J=12.2, 6.7), 7.43(1H, dd, J=10.4, 8.5), 8.31(1H, s) 53 A-53 Et Et Me 2-NH₂-3-Me 1.30(6H, t, J=7.3), 2.23(3H, s), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 5.83(2H, br), 6.67(1H, t, J=7.9), 7.16(1H, d, J=7.9), 7.56(1H, d, J= 7.9), 8.33(1H, s) 54 A-54 Et Et Me 2-NH₂-5-Me 1.30(6H, t, J=7.3), 2.26(3H, s), 2.48(3H, s), 3.37(4H, br), 4.47(2H, s), 5.60(2H, br), 6.69(1H, d, J=8.5), 7.06(1H, d, J=8.5), 7.44(1H, s), 8.32(1H, s) 55 A-55 Et Et Me 2-NH₂-6-Me 1.30(6H, t, J=7.3), 2.45(3H, s), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 5.62(2H, br), 6.57(1H, d, J=7.9), 6.62(1H, d, J=7.9), 7.10(1H, t, J= 7.9), 8.32(1H, s) 56 A-56 Et Et Me 4-NHAc 1.30(6H, t, J=7.1), 2.21(3H, s), 2.47(3H, s), 3.38(4H, br), 4.46(2H, s), 7.63(2H, d, J=8.6), 7.94(2H, d, J= 8.6), 8.31(1H, s) 57 A-57 Et Et H 2-NHAc 1.31(6H, t, J=7.3), 2.32(3H, s), 3.39(4H, br), 4.50(2H, s), 7.14(1H, ddd, J=7.8, 7.6, 1.0), 7.49(1H, ddd, J=8.5, 7.6, 1.5), 7.80(1H, dd, J=7.6, 1.5), 8.43(1H, s), 8.55(1H, s), 8.76(1H, dd, J=8.5, 1.0), 10.83(1H, s) 58 A-58 Et Et Me 2-NHMe 1.30(6H, t, J=7.2), 2.48(3H, s), 2.99(3H, d, J=5.1), 3.38(4H, br), 4.46(2H, s), 6.68(1H, ddd, J=7.9, 7.1, 1.0), 6.74(1H, dd, J=8.5, 1.0), 7.35(1H, ddd, J=8.5, 7.1, 1.5), 7.36(1H, br), 7.67(1H, dd, J=7.9, 1.5), 8.32(1H, s) 59 A-59 Et Et Me 2-NMeAc 1.31(6H, t, J=7.2), 1.75(3H, s), 2.47(3H, s), 3.19(3H, s), 3.38(4H, br), 4.48(2H, s), 7.33(1H, dd, J=7.8, 1.4), 7.50(1H, dt, J=1.4, 7.8), 7.59(1H, dt, J=1.4, 7.8), 8.06(1H, dd, J=7.8, 1.4), 8.33(1H, s)

TABLE 8 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 60 A-60 Et Et Me 2-NHAc-4-F 1.31(6H, t, J=7.3), 2.32(3H, s), 2.48(3H, s), 3.38(4H, br), 4.48(2H, s), 6.84(1H, m), 7.78(1H, dd, J=9.1, 6.1), 8.34(1H, s), 8.60(1H, dd, J=11.6, 2.4), 11.0(1H, s) 61 A-61 Et Et Me 2-NHAc-4-Cl 1.31(6H, t, J=7.3), 2.31(3H, s), 2.48(3H, s), 3.38(4H, br), 4.48(2H, s), 7.12(1H, dd, J=8.5, 1.8), 7.71(1H, d, J=8.5), 8.34(1H, s), 8.88(1H, d, J= 1.8), 10.91(1H, s) 62 A-62 Et Et Me 4-Cl 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 7.46(2H, d, J= 8.5), 7.92(2H, d, J=8.5), 8.32(1H, s) 63 A-63 Et Et Me 2-NH₂-4-Me 1.30(6H, t, J=7.3), 2.29(3H, s), 2.48(3H, s), 3.37(4H, br), 4.46(2H, s), 5.69(2H, s), 6.55(1H, d, J=8.5), 6.58(1H, s), 7.52(1H, d, J=8.5), 8.31(1H, s) 64 A-64 Et Et Me 4-NH₂-2-Cl 1.29(6H, t, J=7.3), 2.47(3H, s), 3.37(4H, br), 4.08(2H, br), 4.45(2H, s), 6.60(1H, dd, J=8.5, 2.5), 6.76(1H, d, J=1.8), 7.70(1H, d, J=8.5), 8.31(1H, s) 65 A-65 Et Et H 2-NH₂-4-F 1.30(6H, t, J=7.3), 3.38(4H, br), 4.47(2H, s), 5.94(2H, br), 6.40- 6.47(2H, m), 7.62(1H, dd, J=9.2, 6.1), 8.40(1H, s), 8.55(1H, s) 66 A-66 Et Et H 4-NHMe 1.30(6H, t, J=7.3), 2.89(3H, d, J= 4.3), 3.38(4H, br), 4.14(1H, s), 4.45(2H, s), 6.62(2H, d, J=9.2), 7.79(2H, d, J=9.2), 8.39(1H, s), 8.54(1H, s) 67 A-67 Et Et H 4-NMe₂ 1.29(6H, t, J=7.3), 3.04(6H, s), 3.38(4H, br), 4.45(2H, s), 6.71(2H, d, J= 9.2), 7.82(2H, d, J=9.2), 8.39(1H, s), 8.54(1H, s) 68 A-68 Et Et H 4-NHEt 1.28(3H, t, J=7.3), 1.29(6H, t, J= 7.3), 3.14-3.27(2H, m), 3.37(4H, br), 3.99(1H, br), 4.45(2H, s), 6.61(2H, d, J= 8.5), 7.77(2H, d, J=8.5), 8.38(1H, s), 8.54(1H, s) 69 A-69 Et Et H 4-NEt₂ 1.20(6H, t, J=7.3), 1.29(6H, t, J= 7.3), 3.41(4H, q, J=7.3), 3.38(4H, br), 4.44(2H, s), 6.67(2H, d, J=9.2), 7.79(2H, d, J=9.2), 8.39(1H, s), 8.54(1H, s)

TABLE 9 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 70 A-70 Me Me Me 2-NH₂ 2.50(3H, s), 2.98(6H, d, J=3.7), 4.49(2H, s), 5.76(2H, br), 6.72(1H, ddd, J=8.1, 7.2, 1.0), 6.77(1H, dd, J= 8.4, 1.0), 7.24(1H, ddd, J=8.4, 7.2, 1.5), 7.64(1H, dd, J=8.1, 1.5), 8.33(1H, s) 71 A-71 Et Et Me 4-NH₂-3-Me 1.29(6H, t, J=7.3), 2.20(3H, s), 2.48(3H, s), 3.37(4H, br), 3.95(2H, s), 4.44(2H, s), 6.66(1H, d, J=8.5), 7.64(2H, d, J=8.5, 1.8), 7.69(1H, s), 8.30(1H, s) 72 A-72 Et Et Me 4-NH₂-3-OMe 1.30(6H, t, J=7.3), 2.48(3H, s), 3.37(4H, br), 3.92(3H, s), 4.17(2H, s), 4.43(2H, s), 6.71(1H, d, J=8.5), 7.37- 7.48(2H, m), 8.30(1H, s) 73 A-73 Et Et Me 4-OMe 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 3.87(3H, s), 4.46(2H, s), 6.98(2H, d, J=8.5), 7.92(2H, d, J= 8.5), 8.31(1H, s) 74 A-74 Et Et Me 4-Me 1.30(6H, t, J=7.3), 2.41(3H, s), 2.48(3H, s), 3.38(4H, br), 4.46(2H, s), 7.28(2H, d, J=8.5), 7.86(2H, d, J= 8.5), 8.32(1H, s) 75 A-75 Et Et Me 2-NH₂-4-NO₂ 1.31(6H, t, J=7.2), 2.49(3H, s), 3.38(4H, br), 4.49(2H, s), 6.17(2H, br), 7.52(1H, dd, J=8.8, 2.1), 7.63(1H, d, J=2.1), 7.79(1H, d, J=8.8), 8.34(1H, s) 76 A-76 Et Et Me 2,4-(NH₂)₂ 1.17(6H, t, J=7.2), 2.35(3H, s), 3.30(4H, br), 4.32(2H, s), 5.43(2H, br), 5.96-5.98(2H, m), 6.25(2H, br), 7.24(1H, d, J=9.3), 8.11(1H, s) (in DMSOd6) 77 A-77 Et Et Me 2-Cl 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.48(2H, s), 7.34- 7.55(3H, m), 7.93(1H, dd, J=7.3, 1.2), 8.33(1H, s) 78 A-78 Et Et Me 2-Me 1.30(6H, t, J=7.3), 2.49(3H, s), 2.68(3H, s), 3.38(4H, br), 4.48(2H, s), 7.28-7.41(3H, m), 7.83(1H, dd, J= 7.9, 1.8), 8.35(1H, s) 79 A-79 Et Et Me 2,3-Cl₂ 1.30(6H, t, J=7.3), 2.48(3H, s), 3.37(4H, br), 4.48(2H, s), 7.56(1H, d, J= 8.5), 7.82(1H, dd, J=8.5, 1.8), 8.06(1H, d, J=1.8), 8.31(1H, s) 80 A-80 Et Et Me 2,4-Cl₂ 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.48(2H, s), 7.37(1H, dd, J=8.5, 2.4), 7.55(1H, d, J=2.4), 7.88(1H, d, J=8.5), 8.33(1H, s)

TABLE 10 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 81 A-81 Et Et Me 4-NH₂-2-F 1.30(6H, t, J=7.3), 2.47(3H, s), 3.37(4H, br), 4.14(2H, s), 4.43(2H, s), 6.45(1H, dd, J=17.1, 2.4), 6.48(1H, dd, J=13.4, 2.4), 7.73(1H, t, J=7.9), 8.32(1H, s) 82 A-82 Et Et Me 4-NO₂ 1.31(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.51(2H, s), 8.17(2H, d, J= 8.5), 8.35(2H, d, J=8.5), 8.33(1H, s) 83 A-83 Et Et Me 4-Ph 1.31(6H, t, J=7.3), 2.49(3H, s), 3.39(4H, br), 4.49(2H, s), 7.36- 7.50(3H, m), 7.63(2H, d, J=6.7), 7.71(2H, d, J=8.5), 8.05(2H, d, J= 8.5), 8.34(1H, s) 84 A-84 Et Et Me 4-COPh 1.31(6H, t, J=7.3), 2.48(3H, s), 3.39(4H, br), 4.50(2H, s), 7.48- 7.67(3H, m), 7.81(2H, dd, J=7.3, 1.2), 7.90(2H, d, J=8.5), 8.10(2H, d, J= 8.5), 8.34(1H, s) 85 A-85 Et Et Me 3,4-(NH₂)₂ 1.15(6H, t, J=7.2), 2.36(3H, s), 3.28(4H, br), 4.37(2H, s), 7.29(1H, d, J= 8.3), 7.62(1H, s), 7.72(1H, d, J= 8.3), 8.13(1H, s) (in DMSOd6) 86 A-86 Et Et Me 4-OMPM 1.30(6H, t, J=7.2), 2.47(3H, s), 3.37(4H, br), 3.82(3H, s), 4.45(2H, s), 5.05(2H, s), 6.93(2H, d, J=8.8), 7.04(2H, d, J=8.8), 7.36(2H, d, J= 8.8), 7.91(2H, d J=8.8), 8.31(1H, s) 87 A-87 Et Et Me 4-NH₂-3- 1.30(6H, t, J=7.2), 2.47(3H, s), OMPM 3.37(4H, br), 4.17(2H, br), 4.44(2H, s), 5.07(2H, s), 6.73(1H, d, J=8.1), 6.93(2H, d, J=8.8), 7.38(2H, d, J= 8.8), 7.41(1H, dd J=8.1, 1.7), 7.52(1H, d, J=1.7), 8.30(1H, s) 88 A-88 Et Et Me 4-OH 1.31(6H, t, J=7.1), 2.48(3H, s), 3.38(4H, br), 4.42(2H, s), 6.86(2H, d, J= 8.5), 7.88(2H, d, J=8.8), 8.45(1H, s) 89 A-89 Et Et Me 4-NH₂-3-OH 1.30(6H, t, J=7.2), 2.50(3H, s), 3.37(4H, br), 4.13(2H, br), 4.31(2H, s), 6.73(1H, d, J=8.1), 7.35(1H, d, J= 1.7), 7.43(1H, dd, J=8.1, 1.7), 8.33(1H, s) 90 A-90 Et Et Me 2-NH₂-4- 1.12(6H, br), 2.37(3H, s), 3.26(4H, br), COOH 4.34(2H, s), 6.87(2H, m), 7.19(1H, dd, J=8.3, 1.5), 7.54(1H, d,=1.5), 7.72(1H, d, J−8.3), 8.09(1H, s) (in DMSOd6) 91 A-91 Et Et Me 4-CO₂tBu 1.30(6H, t, J=7.1), 1.61(9H, s), 2.48(3H, s), 3.38(4H, br), 4.49(2H, s), 8.02(2H, d, J=8.8), 8.08(2H, d, J= 8.8), 8.33(1H, s)

TABLE 11 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 92 A-92 Et Et Me 4-CO₂Me 1.30(6H, t, J=7.1), 2.48(3H, s), 3.38(4H, br), 3.95(3H, s), 4.49(2H, s), 8.05(2H, d, J=8.5), 8.14(2H, d, J= 8.5), 8.32(1H, s) 93 A-93 Et Et Me 4-CONMe₂ 1.30(6H, t, J=7.2), 2.47(3H, s), 2.99(3H, br), 3.13(3H, br), 3.38(4H, br), 4.48(2H, s), 7.53(2H, d, J=8.2), 8.02(2H, d, J=8.2), 8.32(1H, s) 94 A-94 Et Et Me 4-CO₂H 1.12(6H, br), 2.37(3H, s), 3.26(4H, br), 4.36(2H, s), 8.09(2H, d, J=8.3), 8.11(1H, br), 8.13(2H, d, J=8.3) (in DMSOd6) 95 A-95 Et Et Me 2-NH₂-4- 1.30(6H, t, J=7.2), 2.48(3H, s), CO₂Me 3.38(4H, br), 3.92(3H, s), 4.48(2H, s), 5.91(2H, br), 7.35(1H, dd, J=8.3, 1.5), 7.46(1H, d, J=1.5), 7.70(1H, d, J= 8.3), 8.33(1H, s) 96 A-96 Et Et Me 4-NH₂-2-OH 1.30(6H, t, J=7.2), 2.48(3H, s), 3.37(4H, br), 4.02(2H, br), 4.44(2H, s), 6.26(1H, dd, J=8.5, 2.3), 6.32(1H, d, J=2.3), 7.42(1H, d, J=8.5), 8.30(1H, s), 9.94(1H, s) 97 A-97 Et Et Me 4-(1- 1.30(6H, t, J=7.2), 2.04(4H, m), pyrrolidinyl) 2.48(3H, s), 3.35(4H, br), 4.44(2H, s), 6.57(2H, d, J=8.9), 7.81(2H, d, J= 8.9), 8.30(1H, s) 98 A-98 Et Et Me 4-piperidino 1.30(6H, t, J=7.2), 1.68(6H, m), 2.49(3H, s), 3.35(4H, br), 4.44(2H, s), 6.91(2H, d, J=8.9), 7.82(2H, d, J= 8.9), 8.32(1H, s) 99 A-99 Et Et Me 4-O-prenyl 1.30(6H, t, J=7.3), 1.76(3H, s), 1.81(3H, s), 2.47(3H, s), 3.37(4H, br), 4.45(2H, s), 4.57(2H, d, J=6.7), 5.49(1H, t, J=6.7), 6.98(2H, d, J= 9.2), 7.90(2H, d, J=9.2), 8.31(1H, s) 100 A-100 Et Et Me 4-O-i-Pr 1.30(6H, t, J=7.3), 1.36(6H, d, J= 6.1), 2.47(3H, s), 3.37(4H, br), 4.45(2H, s), 4.62(1H, sept, J=6.1), 6.94(2H, d, J=8.5), 7.89(2H, d, J= 8.5), 8.31(1H, s) 101 A-101 Et Et Me 4-OEt 1.29(6H, t, J=7.3), 1.44(3H, t, J= 7.3), 2.47(3H, s), 3.37(4H, br), 4.09(2H, q, J=7.3), 4.45(2H, s), 6.96(2H, d, J=8.5), 7.90(2H, d, J= 8.5), 8.31(1H, s) 102 A-102 Et Et Me 4-SO₂NH₂ 1.30(6H, t, J=7.2), 2.46(3H, s), 3.38(4H, br), 4.46(2H, s), 8.04(2H, d, J= 8.8), 8.10(2H, d, J=8.8), 8.23(1H, s)

TABLE 12 Example Compound ¹H—NMR No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ (δ) ppm 103 A-103 Et Et Me 4-O—Pr 1.05(3H, t, J=7.3), 1.30(6H, t, J= 7.3), 1.83(2H, sext, J=7.3), 2.47(3H, s), 3.37(4H, br), 3.98(2H, t, J=7.3), 4.45(2H, s), 6.96(2H, d, J=9.2), 7.90(2H, d, J=9.2), 8.31(1H, s) 104 A-104 Et Et Me 2-NO₂ 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.46(2H, s), 7.66- 7.79(2H, m), 7.92-8.02(2H, m), 8.30(1H, s) 105 A-105 Et Et Me 4-I 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 7.69(2H, d, J= 8.5), 7.83(2H, d, J=8.5), 8.31(1H, s) 106 A-106 Et Et Me 4-CF₃ 1.31(6H, t, J=7.3), 2.52(3H, s), 3.38(4H, br), 4.49(2H, s), 7.75(2H, d, J= 7.9), 8.11(2H, d, J=7.9), 8.37(1H, s) 107 A-107 Et Et Me H 1.30(6H, t, J=73), 2.48(3H, s), 3.38(4H, br), 4.48(2H, s), 7.43- 7.52(3H, m), 7.96-8.00(2H, m), 8.32(1H, s) 108 A-108 Et Et Me 4-Br 1.30(6H, t, J=7.3), 2.48(3H, s), 3.38(4H, br), 4.48(2H, s), 7.62(2H, d, J= 8.5), 7.85(2H, d, J=8.5), 8.32(1H, s) 109 A-109 Et Et H

1.03(6H, t, J=7.3), 1.67(3H, s), 3.39(4H, br), 3.75-3.81(2H, m), 4.03- 4.09(2H, m), 4.48(2H, s), 7.60(2H, d, J= 8.6), 7.96(2H, d, J=8.6), 8.40(1H, s), 8.54(1H, s) 110 A-110 Et Et H 4-F 1.31(6H, t, J=7.3), 3.39(4H, br), 4.49(2H, s), 7.18(2H, t, J=8.9), 7.97(2H, dd, J=5.3, 8.9), 8.41(1H, s), 8.55(1H, s) 111 A-111 Et CH₂C(Br)═CH₂ H 4-NH₂ 1.31(3H, t, J=7.3), 3.36(2H, t, J= 5.9), 4.07(2H, br), 4.26(2H, br), 4.43(2H, s), 5.61(1H, s), 5.91(1H, s), 6.69(2H, d, J=8.7), 7.55(2H, d, J= 8.7), 8.41(1H, s), 8.55(1H, s) 112 A-112 Et CH₂CH₂OAc H 4-NH₂ 1.32(3H, t, J=7.2), 2.10(3H, s), 3.32(2H, br), 3.68(2H, br), 4.01(2H, br), 4.30(2H, t, J=5.5), 4.45(2H, s), 6.71(2H, d, J=8.8), 7.77(2H, d, J= 8.8), 8.40(1H, s), 8.54(1H, s) 113 A-113 Et CH₂CH₂OH H 4-NH₂ 1.32(3H, t, J=7.5), 3.32(2H, br), 3.62(2H, br), 3.85(2H, t, J=5.0), 4.01(2H, s), 4.45(2H, s), 6.70(2H, d, J= 8.7), 7.76(2H, d, J=8.7), 8.41(1H, s), 8.55(1H, s) 114 A-114 Et Et H 4-Et 1.26(3H, t, J=7.6), 1.30(6H, t, J= 7.6), 2.71(2H, q, J=7.6), 3,38(4H, br), 4.48(2H, s), 7.30(2H, d, J=8.3), 7.89(2H, d, J=8.3), 8.40(1H, s), 8.54(1H, s)

TABLE 13 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 115 A-115 Et Et H 4-i-Pr 1.27(6H, t, J=6.8), 1.30(6H, t, J= 7.3), 2.96(1H, sept., J=6.8), 3.38(4H, br), 4.48(2H, s), 7.33(2H, d, J=8.3), 7.90(2H, d, J=8.3), 8.40(1H, s), 8.54(1H, s) 116 A-116 Et Et H 4-Pr 0.95(3H, t, J=7.3), 1.30(6H, t, J= 7.3), 1.67(2H, sext, J=7.3), 2.64(2H, t, J=7.3), 3.39(4H, br), 4.48(2H, s), 7.28(2H, d, J=8.1), 7.88(2H, d, J= 8.1), 8.40(1H, s), 8.54(1H, s) 117 A-117 Et Et H 4-Ac 1.32(6H, t, J=7.3), 2.66(3H, s), 3.40(4H, br), 4.52(2H, s), 8.06(2H, d, J= 8.7), 8.10(2H, d, J=8.7), 8.43(1H, s), 8.55(1H, s) 118 A-118 Et Et H 4- 1.30(6H, t, J=7.3), 1.46(9H, s), CH₂NHBoc 3.38(4H, br), 4.37(2H, d, J=5.9), 4.48(2H, s), 4.90(1H, br), 7.39(2H, d, J= 8.6), 8.00(2H, d, J=8.6), 8.40(1H, s), 8.57(1H, s) 119 A-119 Et Et H 4-CH₂NH₂ 1.30(6H, t, J=7.3), 3.38(4H, br), 3.94(2H, s), 4.48(2H, s), 7.44(2H, d, J= 8.6), 7.95(2H, d, J=8.6), 8.40(1H, s), 8.54(1H, s) 120 A-120 Et Et H 4-SMe 1.30(6H, t, J=7.3), 2.53(3H, s), 3.38(4H, br), 4.47(2H, s), 7.30(2H, d, J= 8.6), 7.87(2H, d, J=8.6), 8.40(1H, s), 8.54(1H, s) 121 A-121 Et i-Pr H 4-NO₂ 1.30(6H, d, J=6.3), 1.32(3H, t, J= 7.2), 3.35(2H, br), 4.08(1H, br), 4.51(2H, s), 8.17(2H, d, J=9.0), 8.35(2H, d, J=9.0), 8.41(1H, s), 8.54(1H, s) 122 A-122 Et CH₂CH₂ H 4-NO₂ 1.30(3H, t, J=7.2), 3.01(2H, t, J= NH₂ 5.4), 3.42(4H, br), 4.52(2H, s), 8.17(2H, d, J=9.0), 8.35(2H, d, J= 9.0), 8.40(1H, s), 8.53(1H, s) 123 A-123 Et Et H 4-CSNH₂ 1.29(6H, t, J=7.3), 3.26(4H, br), 4.46(2H, s), 7.98(2H, d, J=8.9), 8.02(2H, d, J=8.9), 8.31(1H, s), 8.47(1H, s) (in CDCl₃ + CD₃OD) 124 A-124 Et Et H 4-NO₂, 1.31(6H, t, J=7.3), 3.40(4H, br), -2-MeO 4.08(3H, s), 4.50(2H, s), 7.88-7.94(2H, m), 8.07(1H, d, J=8.3), 8.42(1H, s), 8.55(1H, s) 125 A-125 Et Et H 2,3,5,6-F₄, 1.31(6H, t, J=7.3), 3.38(4H, br), -4-NH₂ 4.41(2H, s), 4.48(2H, s), 8.40(1H, s), 8.54(1H, s) 126 A-126 Et Et H 2-Cl,-4-NO₂ 1.31(6H, t, J=7.1), 3.40(4H, br), 4.53(2H, s), 8.19-8.22(2H, m), 8.40- 8.43(2H, m), 8.55(1H, s)

TABLE 14 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 127 A-127 Pr Pr Me 4-NO₂ 1.04(6H, t, J=7.3), 1.71(4H, sext, J= 7.3), 2.48(3H, s), 3.31(4H, br), 4.50(2H, s), 8.16(2H, d, J=9.0), 8.33(1H, s), 8.35(2H, d, J=9.0) 128 A-128 Bu Bu Me 4-NO₂ 0.98(6H, t, J=7.3), 1.42-1.51(4H, m), 1.61-1.72(4H, m), 2.47(3H, s), 3.35(4H, br), 4.50(2H, s), 8.17(2H, d, J= 9.1), 8.33(1H, s), 8.35(2H, d, J=9.1) 129 A-129 i-Bu i-Bu Me 4-NO₂ 1.03(12H, d, J=6.6), 2.00(2H, sept, J= 6.6), 2.48(3H, s), 3.18(4H, br), 4.49(2H, s), 8.17(2H, d, J=9.0), 8.32(1H, s), 8.35(2H, d, J=9.0) 130 A-130 Et Et i-Pr 4-NO₂ 1.28(6H, d, J=6.8), 1.32(6H, t, J= 7.2), 3.00(1H, sept, J=6.8), 3.39(4H, br), 4.51(2H, s), 8.17(2H, d, J=9.0), 8.34(2H, d, J=9.0), 8.36(1H, s) 131 A-131 Et Et Et 4-NO₂ 1.29(3H, t, J=7.6), 1.31(6H, t, J= 7.6), 2.78(2H, q, J=7.6), 3.39(4H, br), 4.52(2H, s), 8.17(2H, d, J=9.0), 8.35(2H, d, J=9.0), 8.35(1H, s) 132 A-132 Et Et Me 2-F,-4-NO₂ 1.31(6H, dt, J=2.1, 7.1), 2.48(3H, s), 3.38(4H, br), 4.51(2H, d, J=2.7), 7.93-8.27(3H, m), 8.33(1H, s) 133 A-133 Me Et Me 4-NO₂ 1.31(3H, t, J=7.1), 2.49(3H, s), 2.98(3H, s), 3.40(4H, br), 4.52(2H, s), 8.16(2H, d, J=9.1), 8.34(1H, s), 8.35(2H, d, J=9.1) 134 A-134 Et i-Pr Me 4-NO₂ 1.29(6H, d, J=6.4), 1.32(3H, t, J= 7.1), 2.48(3H, s), 3.34(2H, br), 4.10(1H, br), 4.50(2H, s), 8.17(2H, d, J= 9.1), 8.35(2H, d, J=9.1) 135 A-135 Et Pr Me 4-NO₂ 1.05(3H, t, J=7.4), 1.31(3H, t, J= 7.2), 1.71(2H, m), 2.48(3H, s), 3.29(2H, br), 3.40(2H, br), 4.50(2H, s), 8.17(2H, d, J=9.2), 8.33(1H, s), 8.35(2H, d, J=9.2) 136 A-136 Et Bu Me 4-NO₂ 0.98(3H, t, J=7.3), 1.30(3H, t, J= 7.2), 1.47(2H, m), 1.67(2H, m), 2.48(3H, s), 3.32(2H, br), 3.41(2H, br), 4.50(2H, s), 8.17(2H, d, J=9.1), 8.33(1H, s), 8.35(2H, d, J=9.1) 137 A-137 Et Et H 3-NO₂ 1.32(6H, t, J=7.3), 3.40(4H, br), 4.52(2H, s), 7.71(1H, t, J=7.9), 8.34- 8.38(2H, m), 8.42(1H, s), 8.55(1H, s), 8.79(1H, t, J=1.8) 138 A-138 Pr Pr Et 4-NO₂ 1.03(6H, t, J=7.3), 1.29(3H, t, J= 7.6), 1.70(4H, sext, J=7.3), 2.77(2H, q, J=7.6), 3.30(4H, br), 4.51(2H, s), 8.17(2H, d, J=8.9), 8.34(2H, d, J= 8.9), 8.36(1H, s)

TABLE 15 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 139 A-139 Pr Pr Et 4-NH₂ 0.92(6H, t, J=7.3), 1.19(3H, t, J= 7.6), 1.58(4H, sext, J=7.3), 2.63(2H, q, J=7.6), 3.23(4H, br), 4.32(2H, s), 5.92(2H, br), 6.65(2H, d, J=8.6), 7.59(2H, d, J=8.6), 8.15(1H, s) (in DMSOd6) 140 A-140 Pr Pr Et 2-NH₂,-4-F 1.03(6H, t, J=7.3), 1.29(3H, t, J= 7.6), 1.71(4H, sext, J=7.3), 2.77(2H, q, J=7.6), 3.30(4H, br), 4.68(2H, s), 5.93(2H, br), 6.40-6.47(2H, m), 7.62(1H, dd, J=9.2, 6.2), 8.34(1H, s) 141 A-141 Et Et Me 2-OMe,-4-NH₂ 1.29(6H, t, J=7.3), 2.47(3H, s), 3.37(4H, br), 3.90(3H, s), 4.03(2H, s), 4.42(2H, s), 6.26(1H, d, J=2.0), 6.31(1H, dd, J=2.0, 8.2), 7.64(1H, d, J=8.2), 8.30(1H, s) 142 A-142 Pr Pr Me 4-Cl 1.03(6H, t, J=7.3), 1.70(4H, sext, J= 7.3), 2.49(3H, s), 3.30(4H, br), 4.47(2H, s), 7.46(2H, d, J=8.7), 7.92(2H, d, J=8.7), 8.33(1H, s) 143 A-143 Pr Pr Me 4-Me 1.03(6H, t, J=7.4), 1.70(4H, sext, J= 7.4), 2.41(3H, s), 2.47(3H, s), 3.30(4H, br), 4.46(2H, s), 7.28(2H, d, J=7.9), 7.86(2H, d, J=7.9), 8.31(1H, s) 144 A-144 Pr Pr Me 4-NH₂ 1.03(6H, t, J=7.3), 1.70(4H, sext, J= 7.3), 2.47(3H, s), 3.30(4H, br), 4.01(2H, s), 4.43(2H, s), 6.71(2H, d, J= 8.7), 7.77(2H, d, J=8.7), 8.29(1H, s) 145 A-145 Me Me Me 4-NO₂ 2.49(3H, s), 2.99(3H, s), 3.00(3H, s), 4.53(2H, s), 8.16(2H, d, J=9.1), 8.34(1H, s), 8.35(2H, d, J=9.1) 146 A-146 Me Pr Me 4-NO₂ 1.04(6H, t, J=7.4), 1.71(2H, sext, J= 7.4), 2.48(3H, s), 2.99(3H, d, J=4.8), 3.30(2H, br), 4.51(2H, s), 8.16(2H, d, J= 9.1), 8.33(1H, s), 8.35(2H, d, J=7.9) 147 A-147 Me Me Me 4-NH₂ 2.48(3H, s), 2.96(3H, s), 2.98(3H, s), 4.01(2H, br), 4.45(2H, s), 6.70(2H, d, J= 8.7), 7.75(2H, d, J=8.7), 8.30(1H, s) 148 A-148 Me Pr Me 4-NH₂ 1.02(3H, t, J=7.3), 1.69(2H, q, J= 7.3), 2.47(3H, s), 2.97(3H, d, J=4.8), 3.28(2H, br), 4.01(2H, s), 4.44(2H, s), 6.70(2H, d, J=8.7), 7.76(2H, d, J= 8.7), 8.29(1H, s) 149 A-149 Et Pr Et 4-NO₂ 1.04(3H, t, J=7.6), 1.23-1.32(6H, m), 1.71(2H, sext, J=7.6), 2.77(2H, q, J= 7.6), 3.29(2H, br), 3.43(2H, br), 4.51(2H, s), 8.17(2H, d, J=9.2), 8.35(2H, d, J=9.2), 8.36(1H, s)

TABLE 16 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 150 A-150 Me Pr Et 4-NO₂ 1.04(3H, t, J=7.3), 1.29(3H, t, J= 7.6), 1.71(2H, sext, J=7.3), 2.77(2H, q, J=7.6), 3.00(3H, d, J=4.8), 3.30(2H, br), 4.53(2H, s), 8.16(2H, d, J= 8.9), 8.35(2H, d, J=8.9), 8.36(1H, s) 151 A-151 Me Pr Et 4-NH₂ 0.93(3H, t, J=7.3), 1.19(3H, t, J= 7.8), 1.59(2H, sext, J=7.3), 2.64(2H, q, J=7.8), 2.85(3H, d, J=4.5), 3.20(2H, br), 4.34(2H, s), 5.92(2H, br), 6.65(2H, d, J=8.6), 7.58(2H, d, J= 8.6), 8.17(1H, s) (in DMSOd6) 152 A-152 Me Me Et 4-NO₂ 1.29(3H, t, J=7.6), 2.78(2H, q, J= 7.6), 2.99(3H, s), 3.01(3H, s), 4.54(2H, s), 8.16(2H, d, J=9.2), 8.35(2H, d, J= 9.2), 8.37(1H, s) 153 A-153 Me Me Et 4-NH₂ 1.19(3H, t, J=7.8), 2.65(2H, q, J= 7.8), 2.83(3H, s), 2.85(3H, s), 4.35(2H, s), 5.91(2H, br), 6.65(2H, d, J=8.7), 7.58(2H, d, J=8.7), 8.16(1H, s) (in DMSOd6) 154 A-154 Et Et Et 4-NH₂ 1.17(3H, t, J=7.6), 1.20(6H, t, J= 7.6), 2.65(2H, q, J=7.6), 3.29(4H, br), 4.33(2H, s), 5.92(2H, br), 6.65(2H, d, J= 8.6), 7.59(2H, d, J=8.6), 8.16(1H, s) (in DMSOd6) 155 A-155 Pr Pr H 4-NO₂ 1.03(6H, t, J=7.4), 1.71(4H, sext, J= 7.4), 3.31(4H, br), 4.52(2H, s), 8.17(2H, d, J=9.1), 8.33(2H, d, J= 9.1), 8.42(1H, s), 8.54(1H, s) 156 A-156 Pr Pr Me 2-OMe,-4-NH₂ 1.03(6H, t, J=7.2), 1.70(4H, sext, J= 7.2), 2.46(3H, s), 3.30(4H, br), 3.90(3H, s), 4.03(2H, s), 4.41(2H, s), 6.26(1H, d, J=2.0), 6.31(1H, dd, J= 2.0, 8.2), 7.64(1H, d, J=8.2), 8.30(1H, s) 157 A-157 H Pr Me 4-NH₂ 1.03(3H, t, J=7.3), 1.69(2H, sext, J= 7.3), 2.49(3H, s), 3.21(2H, t, J=7.3), 4.02(2H, s), 4.42(2H, s), 6.40(2H, br), 6.71(2H, d, J=8.7), 7.77(2H, d, J= 8.7), 8.32(1H, s) 158 A-158 H Pr Me 4-NO₂ 1.04(3H, t, J=7.3), 1.70(2H, sext, J= 7.3), 2.50(3H, s), 3.24(2H, t, J=7.3), 4.49(2H, s), 6.46(2H, br), 8.16(2H, d, J= 9.1), 8.35(2H, d, J=9.1), 8.36(1H, s)

TABLE 17 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ Salt ¹H-NMR (δ) ppm 159 A-159 Me Me Me 4-NO₂ HCl 2.46(3H, s), 2.92(6H, br), 4.44(2H, s), 8.10(1H, s), 8.24(2H, d, J=9.2), 8.42(2H, d, J=9.2) (in CD₃OD) 160 A-160 n-Pr n-Pr Me 4-NH₂ 2HCl 0.96(6H, br), 1.65(4H, br), 2.45(3H, s), 3.25(4H, br), 3.35(2H, br), 4.39(2H, s), 7.41(2H, d, J=8.9), 8.05(2H, d, J= 8.9), 8.07(1H, s) (in CD₃OD) 161 A-161 Et Et Me 2-OMe- — 1.31(6H, t, J=7.3), 2.48(3H, s), 4-NO₂ 3.39(4H, br), 4.07(3H, s), 4.48(2H, s), 7.88-7.94(2H, m), 8.07(1H, d, J=8.2), 8.33(1H, s) 162 A-162 Me Me Me 2-OMe- — 2.50(3H, s), 3.00(6H, d, J=4.0), 4-NO₂ 4.07(3H, s), 4.51(2H, s), 7.88- 7.94(2H, m), 8.07(1H, d, J=7.9), 8.35(1H, s) 163 A-163 Me Et Me 4-NO₂ HCl 1.11(3H, br), 2.39(3H, br), 2.75(3H, br), 3.30(2H, br), 4.38(2H, s), 8.13(1H, s), 8.24(2H, d, J=9.1), 8.43(2H, d, J=9.1) (in DMSOd6) 164 A-164 Me n-Pr Me 4-NO₂ HCl 0.86(3H, br), 1.52(2H, br), 2.39(3H, br), 2.80(3H, br), 3.15(2H, br), 4.38(2H, s), 8.13(1H, s), 8.24(2H, d, J=9.1), 8.43(2H, d, J=9.1) (in DMSOd6) 165 A-165 i-Pr i-Pr Me 4-NO₂ — 1.30(12H, d, J=6.4), 2.47(3H, s), 4.00(2H, br), 4.49(2H, s), 8.17(2H, d, J=9.1), 8.32(1H, s), 8.35(2H, d, J=9.1) 166 A-166 i-Pr i-Pr Me 4-NH₂ — 1.29(12H, d, J=6.4), 2.46(3H, s), 4.00(2H, br), 4.01(2H, s), 4.42(2H, s), 6.71(2H, d, J=8.9), 7.77(2H, d, J=8.9), 8.29(1H, s) 167 A-167 Et n-Pr Me 4-NH₂ — 1.04(3H, t, J=7.5), 1.29(3H, t, J= 7.3), 1.70(2H, q, J=7.2), 2.47(3H, s), 3.28(2H, br), 3.40(2H, br), 4.01(2H, s), 4.43(2H, s), 6.71(2H, d, J=8.7), 7.77(2H, d, J=8.7), 8.29(1H, s) 168 A-168 Me Et Me 4-NH₂ — 1.29(3H, t, J=7.3), 2.48(3H, s), 2.96(3H, d, J=4.8), 3.40(2H, br), 4.00(2H, s), 4.45(2H, s), 6.71(2H, d, J=8.8), 7.77(2H, d, J=8.8), 8.30(1H, s)

TABLE 18 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ Salt ¹H-NMR (δ) ppm 169 A-169 n-Bu n-Bu Me 4-NH₂ — 0.97(6H, t, J=7.2), 1.46(4H, q, J= 7.1), 1.55-1.73(4H, m), 2.46(3H, s), 3.33(4H, br), 4.00(2H, s), 4.43(2H, s), 6.71(2H, d, J=8.8), 7.77(2H, d, J=8.8), 8.29(1H, s) 170 A-170 Me i-Pr Me 4-NO₂ — 1.30(6H, d, J=6.4), 2.49(3H, s), 2.96(3H, d, J=4.9), 4.10(1H, br), 4.51(2H, s), 8.17(2H, d, J=9.1), 8.33(1H, s), 8.35(2H, d, J=9.1) 171 A-171 Me i-Pr Me 4-NH₂ — 1.28(6H, d, J=6.4), 2.48(3H, s), 2.95(3H, d, J=4.9), 4.01(2H, s), 4.10(1H, br), 4.44(2H, s), 6.71(2H, d, J=8.7), 7.77(2H, d, J= 8.7), 8.30(1H, s) 172 A-172 Et Et H 4-NO₂ — 1.31(6H, t, J=7.1), 3.40(4H, br), 4.52(2H, s), 8.17(2H, d, J=9.1), 8.35(2H, d, J=9.1), 8.42(1H, s), 8.55(1H, s) 173 A-173 Me Me H 4-NO₂ — 3.01(6H, d, J=4.8), 4.54(2H, s), 8.16(2H, d, J=9.1), 8.35(2H, d, J= 9.1) 8.43(1H, s), 8.55(1H, s) 174 A-174 Me Me H 4-NH₂ — 2.99(6H, d, J=4.6), 4.01(2H, br), 4.48(2H, s), 6.71(2H, d, J=8.7), 7.76(2H, d, J=8.7), 8.40(1H, s), 8.53(1H, s) 175 A-175 Et CF₃CH₂ Me 4-NO₂ — 1.38(3H, t, J=7.3), 2.51(3H, s), 3.30-3.38(2H, m), 4.23(2H, q, J= 7.3), 4.52(2H, s), 8.17(2H, d, J= 9.1), 8.35(2H, d, J=9.1), 8.40(1H, s) 176 A-176 Me Et H 4-NH₂ — 1.29(3H, t, J=7.3), 2.97(3H, d, J= 4.9), 3.42(2H, br), 4.00(2H, br), 4.46(2H, s), 6.71(2H, d, J=8.7), 7.77(2H, d, J=8.7), 8.39(1H, s), 8.54(1H, s) 177 A-177 Me Et H 4-NO₂ — 1.31(3H, t, J=7.3), 2.99(3H, d, J= 4.5), 3.45(2H, br), 4.53(2H, s), 8.17(2H, d, J=8.9), 8.35(2H, d, J= 8.9), 8.43(1H, s), 8.55(1H, s) 178 A-178 Et n-Pr H 4-NH₂ — 1.02(3H, t, J=7.4), 1.30(3H, t, J= 7.2), 1.70(2H, q, J=7.3), 3.29(2H, br), 3.40(2H, br), 4.01(2H, s), 4.45(2H, s), 6.71(2H, d, J=8.6), 7.77(2H, d, J=8.6), 8.38(1H, s), 8.53(1H, s) 179 A-179 Et n-Pr H 4-NO₂ — 1.03(3H, t, J=7.4), 1.31(3H, t, J= 7.3), 1.71(2H, q, J=7.3), 3.30(2H, br), 3.40(2H, br), 4.52(2H, s), 8.17(2H, d, J=9.2), 8.35(2H, d, J=9.2), 8.42(1H, s), 8.55(1H, s)

TABLE 19 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ Salt ¹H-NMR (δ) ppm 180 A-180 Et n-Bu Me 4-NH₂ — 0.98(3H, t, J=7.3), 1.29(3H, t, J= 7.3), 1.47(2H, q, J=7.4), 1.63- 1.69(2H, m), 2.47(3H, s), 3.30(2H, br), 3.39(2H, br), 4.01(2H, s), 4.43(2H, s), 6.71(2H, d, J=8.7), 7.77(2H, d, J=8.7), 8.30(1H, s) 181 A-181 Et CH₂CH═ Me 4-NO₂ — 1.30(3H, t, J=7.1), 2.49(3H, s), CH₂ 3.40(2H, br), 4.01(2H, br), 4.51(2H, s), 5.30(2H, dd, J=17.3, 10.2), 5.97(1H, ddt, J=17.3, 10.2, 5.4), 8.16(2H, d, J=8.5), 8.35(2H, d, J=8.5), 8.35(1H, s) 182 A-182 Et i-Pr Me 4-NH₂ — 1.28(6H, d, J=6.4), 1.31(3H, t, J= 7.3), 2.47(3H, s), 3.33(2H, br), 4.01(3H, br), 4.43(2H, s), 6.71(2H, d, J=8.7), 7.77(2H, d, J= 8.7), 8.29(1H, s) 183 A-183 Et CH₂C≡ Me 4-NO₂ — 1.34(3H, t, J=7.3), 2.33(1H, br), CH 2.50(3H, s), 3.36(2H, br), 4.23(2H, br), 4.53(2H, s), 8.17(2H, d, J=9.2), 8.35(2H, d, J= 9.2), 8.38(1H, s) 184 A-184 H Et Me 4-NH₂ — 1.11(3H, t, J=7.1), 2.36(3H, s), 3.30(2H, br), 4.33(2H, s), 5.93(2H, br), 6.65(2H, d, J=7.3), 7.59(2H, d, J=7.3), 8.15(1H, s) 185 A-185 H Et Me 4-NO₂ — 1.32(3H, t, J=7.3), 2.50(3H, s), 3.32(2H, br), 4.49(2H, s), 8.16(2H, d, J=9.1), 8.35(2H, d, J= 9.1), 8.36(1H, s)

TABLE 20 Example Compound No. No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ Salt ¹H-NMR (δ) ppm 186 A-186 Et Et Me 4-NH₂ 2HCl 1.09(6H, t, J=7.1), 2.28(3H, s), 3.04(4H, br), 4.20(2H, s), 7.39(2H, d, J=8.9), 7.83(1H, s), 7.93(2H, d, J=8.9) (in CD₃OD) 187 A-187 Et Et Me 4-NO₂ HCl 1.24(6H, br), 2.44(3H, s), 4.42(2H, 2H, s), 8.07(1H, s), 8.24(2H, d, J=9.1), 8.42(2H, d, J= 9.1) (in CD₃OD) 188 A-188 Et Pr Me 4-NO₂ HCl 0.97(3H, br), 1.22(6H, br), 1.65(2H, br), 2.43(3H, s), 3.30(2H, br), 3.40(2H, br), 4.41(2H, s), 8.07(1H, s), 8.22(2H, d, J=9.1), 8.41(2H, d, J=9.1) (in CD₃OD) 189 A-189 Et Et Me 2-MeO, HCl 1.23(6H, br), 2.46(3H, s), 4-NH₂ 4.00(3H, s), 4.41(2H, s), 6.89(1H, dd, J=1.8, 8.4), 6.95(1H, d, J= 1.8), 7.87(1H, d, J=8.4), 8.07(1H, s) (in CD₃OD)

TABLE 21

or

Exam- Com- ple pound No. No. R¹⁶ R¹⁷ R¹⁸ ¹H-NMR (δ) ppm 190 A-190 Et H 4-NO₂ 1.24(3H, t, J=7.2), 3.05(6H, s), 3.28(2H, dq, J=7.2, 5.1), 4.50(2H, s), 8.03(1H, br), 8.17(2H, d, J=9.0), 8.36(2H, d, J=9.0), 8.39(1H, s), 8.53 (1H, s)

Example 191 Synthesis of Compound B-1

To a solution of 2-(2-aminophenyl)-5-mercaptooxadiazole (2.0 g) in 50 ml of methanol were added 600 mg of potassium hydroxide and 1.48 g of methyl iodide and the mixture was stirred for 1 h at room temperature. Methanol was removed and dichloromethane was added. The organic layer was washed with water and purified by column chromatography on silica gel to give 1.87 g of 2-(2-aminophenyl)-(5-methylthio)oxadiazole.

¹H-NMR: (CDCl₃) 2.78(3H, s), 5.76(2H, br), 6.74(1H, dt, J=1.0, 7.8 Hz), 6.78(1H, dd, J=7.8, 1.0 Hz), 7.26(1H, dt, J=1.5, 7.8 Hz), 7.69(1H, dd, J=1.5, 7.8 Hz).

To a solution of 2-(2-aminophenyl)-5-(methylthio)oxadiazole (1.8 g) in methoxyethanol was added 4.4 g of hydrazine hydrate and the mixture was stirred for 30 h at 120° C. The solvent and excess hydrazine were removed and the residue was purified by column chromatography on silica gel to give 613 mg of 2-(2-aminophenyl)-5-hydrazinooxadiazole.

¹H-NMR (CDCl₃): 4.04(2H, br), 5.44(2H, br), 6.66(1H, dt, J=1.4, 7.8 Hz), 6.69(1H, dd, J=7.8, 1.4 Hz), 7.23(1H, dt, J=1.4, 7.8 Hz), 7.23(1H, br), 7.29(1H, dd, J=7.8, 1.4 Hz).

Compound 5 (100 mg) was dissolved in 25% solution of hydrogen bromide in acetic acid (3 ml) and the mixture was stirred overnight at 40° C. The solvent was removed under reduced pressure and the residue was dissolved in 3 ml of methanol. To the solution was added 180 mg of 2-(2-aminophenyl)-5-hydrazino-oxadiazole and the mixture was stirred for 4 h. After a half amount of methanol was removed, the residual mixture was purified by the use of silica gel column chromatography gave 55 mg of compound II-1. The physical data was shown in Table 22.

Example 192 Synthesis of Compound B-2

To a solution of 2-aminobenzoic hydrazide (1.0 g) in 30 ml of THF was added 1.3 g of carbonyldimidazole and the mixture was heated at reflux for 15 h. The solvent was removed under reduced pressure and the residue was crystallized from aqueous ethanol to give 809 mg of 2-(2-aminophenyl)-5-oxadiazolinone.

¹H-NMR(DMSOd₆): 6.30(2H, br), 6.64(1H, ddd, J=7.9, 7.0, 0.9 Hz), 6.84(1H, dd, J=8.6, 0.9 Hz), 7.22(1H, ddd, J=8.6, 7.0, 1.5 Hz), 7.44(1H, dd, J=7.9, 1.5 Hz), 12.50(1H, br).

Compound 5 (200 mg) was dissolved in 25% solution of hydrogen bromide in acetic acid (1 ml) and the mixture was stirred overnight at 40° C. The solvent was removed under reduced pressure and the residue was dissolved in 1 ml of DMF. The mixture was added to a solution of 320 mg of 2-(2-aminophenyl)-5-oxadiazolinone and 75 mg of sodium hydride in 5 ml of DMF at ice-cooling. The reaction mixture was stirred for 1 h at room temperature and water was added to the mixture. The mixture was extracted with dichloromethane and the organic layer was washed with brine and dried. Purification by the use of silica gel column chromatography gave 40 mg of desired compound. The physical data was shown in Table 22.

Example 193 Synthesis of Compound B-3

To a solution of 1-(2-aminobenzoyl)thiosemicarbazide (1.3 g) in 30 ml of methanol was added 1.52 g of red mercuric oxide and the mixture was heated at reflux for 5 h. The insoluble material was removed by filtration and filtrate was concentrated in vacuo. The residue was purified by column chromatography on silica gel to give 645 mg of 2-amino-5-(2-aminophenyl)oxadiazole.

¹H-NMR(DMSOd₆): 6.53(2H, br), 6.62(1H, t, J=7.8 Hz), 6.83(1H, d, J=7.8 Hz), 7.16(1H, dt, J=1.6, 7.8 Hz), 7.16(2H, br), 7.43(1H, dd, J=7.8, 1.6 Hz).

Using 2-amino-5-(2-aminophenyl)oxadiazole as a starting material, compound B3 (33 mg) was obtained in a manner similar to that described in Example 192. The physical data was shown in Table 22.

Example 194 Synthesis of Compound B-4

To a solution of 2-aminobenzoic hydrazide (1.5 g) in DMF was added 0.7 g of methyl isothiocyanate and the mixture was stand for a day. The solvent was removed and chloroform was added to the residue to give 2.1 of 1-(2-aminobenzoyl) 4-methylthiosemicarbazide as a precipitate.

¹H-NMR(DMSOd₆): 2.87(3H, d, J=4.3 Hz), 6.51(1H, t, J=7.8 Hz), 6.71(1H, d, J=7.8 Hz), 7.18(1H, t, J=7.8 Hz), 7.64(1H, d, J=7.8 Hz), 7.95(1H, br).

Condensation with pyrimidine derivative which was carried out in a manner similar to that described in Example 191 gave compound B-4. The physical data was shown in Table 22.

TABLE 22

or

Exam- Com- ple pound No. No. X ¹H-NMR (δ) ppm 191 B-1 —NHNH— 1.14(3H, t, J=7.2), 2.37(3H, s), 2.82 (3H, d, J=4.6), 3.26(2H, dq, J=5.6, 7.2), 4.21(2H, s), 6.56(1H, ddd, J=7.8, 7.1, 1.0), 6.68(1H, dd, J=8.7, 1.0), 7.22(1H, ddd, J=8.7, 7.1, 1.4), 7.47(1H, dd, J= 7.8, 1.4), 7.76(1H, s) (in DMSOd6) 192 B-2 —O— 1.27(3H, t, J=7.1), 2.49(3H, s), 2.96 (3H, d, J=4.9), 3.39(2H, br), 4.95(2H, s), 5.22(2H, br), 6.69(1H, dd, J=8.3, 0.7), 6.72(1H, ddd, J=8.1, 7.0, 0.7), 7.21(1H, ddd, J=8.3, 7.0, 1.5), 7.61 (1H, dd, J=8.1, 1.5), 8.16(1H, s) 193 B-3 —NH— 1.34(3H, t, J=7.1), 2.50(3H, s) 2.99(3H, d, J=4.2), 3.40(2H, br), 4.46(2H, d, J=2.9), 5.72 (2H, br), 6.70(1H, ddd, J=7.8, 7.3, 1.0), 6.74(1H, dd, J=8.3, 1.0), 6.75(1H, br), 7.18(1H, ddd, J=8.3, 7.3, 1.5), 7.55 (1H, dd, J=7.8, 1.5), 8.21(1H, s) 194 B-4 —NMe— 1.20(3H, t, J=6.8), 2.50(3H, s), 2.89 (3H, d, J=4.6), 3.11(3H, s), 3.29(2H, br), 4.68(2H, s), 5.74(2H, br), 6.70(1H, ddd, J=7.8, 7.3, 0.7), 6.75(1H, dd, J= 8.3, 0.7), 7.17(1H, ddd, J=8.3, 7.8, 1.5), 7.58(1H, dd, J=7.8, 1.5), 8.14 (1H, s)

Example 195-Example 196

Compound (C-1) and compound (C-2) were synthesized in a manner similar to those described in Example 1 to Example 190. The physical data were shown in Table 23.

TABLE 23

Exam- Com- ple pound No. No. R¹⁹ ¹H-NMR (δ) ppm 195 C-1 Me 1.27(6H, t, J=7.1), 2.57(3H, s), 3.36(4H, br), 4.70(2H, s), 5.78(2H, br), 6.73(1H, ddd, J=8.1, 6.8, 1.1), 6.78(1H, dd, J=8.3, 1.1), 7.25(1H, ddd, J=8.3, 6.8, 1.5), 7.65(1H, dd, J=8.1, 1.5), 8.45(1H, s) 196 C-2 Et 1.27(6H, t, J=7.1), 1.28(3H, t, J=7.6), 2.87(2H, q, J=7.6), 3.36(4H, br), 4.72(2H, s), 5.78(2H, br), 6.73(1H, t, J=7.7), 6.78(1H, d, J=7.7), 7.26(1H, td, J=7.7, 1.5), 7.66(1H, dd, J=7.7, 1.5), 8.51(1H, s)

Example 197 Synthesis of Compound D-1

A mixture of 2-aminonicotinic acid methylester (0.97 g) and 1.81 g of hydrazine hydrate was heated for 2 h at 100° C. Excess hydrazine was removed under reduced pressure and the residue was suspended in 20 ml of ethanol. To the suspension were added 1.65 g of carbon disulfide and 2.19 g of triethylamine and the mixture was heated for 15 h. Ethanol was removed and water was added to the reside. After removal of the insoluble material, the mixture was neutralized by adding aqueous potassium hydrogen sulfate and the precipitate was collected to give 0.51 g of 2-(2-aminopyridine-3-yl)-5-mercaptooxadiazole.

¹H-NMR (CDCl₃+CD₃OD): 6.77(1H, dd, J=7.8, 4.9 Hz), 8.06(1H, dd, J=7.8, 1.2), 8.19(1H, dd, J=4.9, 1.2 Hz).

Compound 10 (200 mg) was dissolved in 25% solution of hydrogen bromide in acetic acid (1 ml) and the mixture was stirred overnight at 40° C. The solvent was removed under reduced pressure and the residue was dissolved in 2 ml of DMF. The mixture was added to a solution of 332 mg of 2-(2-aminopyridine-3-yl)-5-mercapto-1,3,4-oxadiazole and 68 mg of sodium hydride in 2 ml of DMF at ice-cooling. After stirring for 1 h at room temperature, water was added to the mixture. The resulting mixture was extracted with dichloromethane and the organic layer was washed with brine and dried. Purification by use of silica gel column chromatography gave 182 mg of compound D-1. The physical data was shown in Table 24.

Example 198-Example 241

Compound D-2 to compound D-45 were synthesized in a manner similar to those described in Example 1 to Example 190 and Example 197. The physical data were shown in Tables 24 to 27.

TABLE 24

or

Example Compound No. No. R¹⁶ R¹⁷ Z ¹H-NMR (δ) ppm 197 D-1  Et Me

1.30(6H, t, J=7.2), 2.48(3H, s), 3.38(4H, br), 4.47(2H, s), 6.48(1H, br), 6.70(1H, dd, J=7.8, 4.8), 7.90(1H, dd, J=7.8, 2.0), 8.19(1H, dd, J= 7.8, 2.0), 8.32(1H, s) 198 D-2  Me Me

1.30(3H, t, J=7.2), 2.49(3H, s), 2.98(3H, d, J= 4.6), 3.41(2H, br), 4.51(2H, s), 7.43(1H, dd, J= 8.1, 4.9), 8.27(1H, dt, 8.1, 2.0), 8.33(1H, s), 8.74(1H, dd, J=4.9, 2.0), 9.19(1H, d, J=2.0) 199 D-3  Et Me

1.17(6H, t, J=7.2), 2.35(3H, s), 2.43(3H, s), 3.30(4H, dq, J=5.4, 7.2), 4.40(2H, s), 7.56(2H, br), 8.16(1H, s), 8.59(1H, s) (in DMSOd6) 200 D-4  Et Me

1.30(6H, t, J=7.3), 2.49(3H, s), 3.38(4H, br), 4.51(2H, s), 5.73(2H, br), 7.08(1H, s), 7.20(1H, m), 7.40(1H), 7.56(1H, d, J=7.9), 7.72(1H, d, J=7.9), 8.23(1H, s), 8.36(1H, s) 201 D-5  Et Me

1.30(6H, t, J=7.3), 2.48(3H, s), 3.37(4H, br), 4.50(2H, s), 6.58(2H, br), 8.03(1H, d, J=2.5), 8.16(1H, d, J=2.5), 8.35(1H, s) 202 D-6  Et Me

1.30(6H, t, J=7.2), 2.47(3H, s), 3.37(4H, br), 4.45(2H, s), 4.80(2H, br), 6.55(1H, dd, J=8.5, 0.7), 8.00(1H, dd, J=8.5, 2.3), 8.30(1H, s), 8.65(1H, dd, J=2.3, 0.7) 203 D-7  Et Me

1.30(6H, t, J=7.2), 2.48(3H, s), 3.37(4H, br), 4.42(2H, s), 4.93(2H, br), 7.72(1H, s), 8.29(1H, s) 204 D-8  Et Me

1.30(6H, t, J=7.1), 2.47(3H, s), 3.37(4H, br), 4.41(2H, s), 5.39(2H, br), 6.62(1H, d, J=5.2), 7.27(1H, d, J=5.2), 8.30(1H, s) 205 D-9  Et H

1.30(6H, t, J=7.3), 3.38(4H, br), 4.47(2H, s), 7.43(1H, dd, J=4.9, 3.0), 7.61(1H, dd, J=4.9, 1.3), 7.94(1H, dd, J=3.0, 1.3), 8.40(1H, s), 8.54(1H, s) 206 D-10 Et H

1.30(6H, t, J=7.3), 2.62(3H, s), 3.39(4H, br), 4.46(2H, s), 6.71(1H, d, J=2.0), 7.33(1H, d, J= 2.0), 8.39(1H, s), 8.54(1H, s) 207 D-11 Et H

1.30(6H, t, J=7.3), 2.28(3H, s), 2.56(3H, s), 3.38(4H, br), 4.44(2H, s), 6.28(1H, s), 8.38(1H, s), 8.54(1H, s) 208 D-12 Et H

1.30(6H, t, J=7.3), 3.38(4H, br), 4.48(2H, s), 6.57(1H, dd, J=3.6, 2.0), 7.08(1H, dd, J=3.6, 1.0), 7.61(1H, dd, J=2.0, 1.0), 8.39(1H, s), 8.54(1H, s) 209 D-13 Et H

1.30(6H, t, J=7.3), 3.39(4H, br), 4.48(2H, s), 6.50(1H, d, J=3.5), 7.03(1H, d, J=3.5), 8.38(1H, s), 8.54(1H, s) 210 D-14 Et H

1.30(6H, t, J=7.3), 2.58(3H, s), 3.39(4H, br), 4.46(2H, s), 6.96(1H, d, J=4.9), 7.38(1H, d, J= 4.9), 8.41(1H, s), 8.54(1H, s)

TABLE 25 Example Compound No. No. R¹⁶ R¹⁷ Z ¹H-NMR (δ) ppm 211 D-15 Et H

1.30(6H, t, J=7.3), 2.54(3H, s), 3.38(4H, br), 4.45(2H, s), 6.79(1H, d, J=4.0), 7.46(1H, d, J= 4.0), 8.38(1H, s), 8.54(1H, s) 212 D-16 Et H

1.30(6H, t, J=7.3), 3.39(4H, br), 4.06(3H, s), 4.51(2H, s), 8.28(1H, s), 8.40(1H, s), 8.54(1H, s) 213 D-17 Et H

1.31(6H, t, J=7.3), 3.40(4H, br), 4.13(3H, s), 4.51(2H, s), 8.20(1H, s), 8.41(1H, s), 8.55(1H, s) 214 D-18 Et H

1.31(6H, s), 3.39(4H, br), 4.52(2H, s), 7.27(1H, d, J=4.0), 7.43(1H, d, J=4.0), 8.40(1H, s), 8.55(1H, s) 215 D-19 Et H

1.16(6H, t, J=7.3), 3.31(4H, br), 4.40(2H, s), 7.38(1H, s), 8.26(1H, s), 8.44(1H, s) (in DMSOd6) 216 D-20 Et H

1.16(6H, t, J=7.3), 3.30(4H, br), 4.42(2H, s), 8.25(1H, s), 8.43(1H, s), 9.04(1H, s) (in DMSOd6) 217 D-21 Et H

1.30(6H, t, J=7.3), 3.38(4H, br), 4.47(2H, s), 7.43(1H, dd, J=4.9, 3.0), 7.60(1H, dd, J=4.9, 1.3), 7.94(1H, dd, J=3.0, 1.3), 8.40(1H, s), 8.54(1H, s) 218 D-22 Et H

1.16(6H, t, J=7.3), 3.30(4H, br), 4.42(2H, s), 8.25(1H, s), 8.43(1H, s), 9.04(1H, s) (in DMSOd6) 219 D-23 Et H

1.16(6H, t, J=7.3), 3.31(4H, br), 4.40(2H, s), 7.38(1H, s), 8.26(1H, s), 8.44(1H, s) (in DMSOd6) 220 D-24 Et H

1.31(6H, t, J=7.3), 3.39(4H, br), 4.52(2H, s), 7.27(1H, d, J=4.0), 7.43(1H, d, J=4.0), 8.40(1H, s), 8.55(1H, s) 221 D-25 Et H

1.16(6H, t, J=7.3), 3.31(4H, quint, J=7.3), 4.00(3H, s), 4.43(2H, s), 7.13(1H, s), 8.26(1H, s), 8.43(1H, s) (in DMSOd6) 223 D-26 Et H

1.16(6H, t, J=6.9), 2.48(3H, s), 3.32(4H, quint, J=6.9), 4.36(2H, s), 7.69(1H, s), 8.22(1H, s), 8.42(1H, s) (in DMSOd6) 223 D-27 Et H

1.16(6H, t, J=7.1), 2.20(3H, s), 2.22(3H, s), 3.31(4H, quint, J=7.1), 4.36(2H, s), 5.80(1H, d, J=2.0), 8.20(1H, s), 8.42(1H, s), 11.32(1H, br) (in DMSOd6)

TABLE 26 Example Compound No. No. R¹⁶ R¹⁷ Z ¹H-NMR (δ) ppm 224 D-28 Et H

1.32(6H, t, J=7.1), 3.41(4H, br), 4.54(2H, s), 8.22(1H, d, J=8.9), 8.40-8.45(1H, m), 8.55(1H, s), 8.67(1H, d, J=1.8), 8.92(2H, dd, J=1.8, 4.3) 225 D-29 Et H

1.30(6H, t, J=7.3), 2.64(3H, s), 3.39(4H, br), 4.50(2H, s), 7.28(1H, d, J=8.1), 8.16(1H, dd, J=8.1, 2.3), 8.41(1H, s), 8.54(1H, s), 9.06(1H, d, J=2.3) 226 D-30 Et H

1.30(6H, t, J=7.3), 3.38(4H, br), 4.46(2H, s), 6.87(1H, dd, J=1.5, 0.8), 7.51(1H, t, J=0.8), 8.01(1H, dd, J=1.5, 0.8), 8.38(1H, s), 8.54(1H, s) 227 D-31 Et H

1.15(6H, t, J=7.1), 3.31(4H, br), 4.40(2H, s), 6.72(1H, s), 8.26(1H, s), 8.43(1H, s) (in DMSOd6) 228 D-32 Et H

1.30(6H, t, J=7.3), 2.67(3H, s), 3.39(4H, br), 4.53(2H, s), 8.43(1H, s), 8.54(1H, s), 8.57(1H, d, J=1.0), 9.28(1H, d, J=1.0) 229 D-33 Et H

1.17(6H, t, J=7.3), 3.30(4H, br), 4.44(2H, s), 7.61(1H, dd, J=7.9, 4.8), 8.32(1H, s), 8.42(1H, d, J=7.9), 8.45(1H, s), 8.70(1H, s), 8.74(1H, d, J=4.8), 9.23(1H, d, J=2.1) (in DMSOd6) 230 D-34 Et H

1.31(6H, t, J=7.3), 3.40(4H, br), 4.52(2H, s), 7.90(2H, d, J=6.3), 8.17(1H, s), 8.43(1H, s), 8.55(1H, s), 8.77(2H, d, J=6.3) 231 D-35 Et H

1.30(6H, t, J=7.3), 3.39(4H, br), 4.50(2H, s), 6.40(2H, t, J=2.3), 7.40(1H, d, J=8.6), 7.57(2H, t, J=2.3), 8.31(1H, dd, J=8.6, 2.3), 8.42(1H, s), 8.55(1H, s), 8.97(1H, dd, J=2.3, 1.0). 232 D-36 Et Me

1.31(6H, t, J=7.3), 2.29(3H, s), 2.48(3H, s), 3.38(4H, br), 4.44(2H, s), 7.45(1H, d, J=5.3), 8.19(1H, d, J=5.3), 8.33(1H, s), 10.02(1H, br) 233 D-37 Et H

1.31(6H, t, J=7.3), 3.39(4H, br), 4.50(2H, s), 5.76(2H, br), 7.44(1H, d, J=5.3), 8.00(1H, d, J= 5.3), 8.28(1H, s), 8.42(1H, s), 8.55(1H, s) 234 D-38 Et H

1.31(6H, t, J=7.3), 3.39(4H, br), 4.46(2H, s), 6.69(1H, dd, J=8.9, 1.7), 7.99-8.04(2H, m), 8.38(1H, s), 8.54(1H, s), 11.73(1H, br) 235 D-39 Et H

1.31(6H, t, J=7.3), 3.39(4H, br), 4.00(3H, s), 4.49(2H, s), 6.84(1H, d, J=8.9), 8.14(1H, dd, J=8.9, 2.3), 8.40(1H, s), 8.55(1H, s), 8.74(1H, d, J=2.3) 236 D-40 Et H

1.31(6H, t, J=7.3), 3.39(4H, br), 3.62(3H, s), 4.46(2H, s), 6.66(1H, d, J=9.6), 7.86(1H, dd, J=9.6, 2.3), 8.04(1H, d, J=2.3), 8.38(1H, s), 8.54(1H, s)

TABLE 27 Example Compound No. No. R¹⁶ R¹⁷ Z ¹H-NMR (δ) ppm 237 D-41 Et H

1.31(6H, t, J=7.1), 3.39(4H, br), 4.51(2H, s), 7.83(2H, d, J=6.1), 8.42(1H, s), 8.55(1H, s), 8.78(2H, d, J=6.1) 238 D-42 Et H

1.31(6H, t, J=7.1), 3.39(4H, br), 4.50(2H, s), 7.83(2H, d, J=7.4), 8.25(2H, d, J=7.4), 8.40(1H, s), 8.55(1H, s) 239 D-43 Et H

1.31(6H, t, J=7.3), 3.39(4H, br), 4.49(2H, s), 8.08(1H, d, J=1.8), 8.35(1H, d, J=1.8), 8.40(1H, s), 8.55(1H, s) 240 D-44 Et H

1.30(6H, t, J=7.3), 3.38(4H, br), 3.91(2H, br), 4.46(2H, s), 6.67(2H, d, J=8.6), 6.76(1H, d, J= 16.3), 7.32(1H, d, J=16.3), 7.34(2H, d, J=8.6), 8.39(1H, s), 8.54(1H, s) 241 D-45 Et Me

1.31(6H, t, J=7.3), 2.48(3H, s), 3.39(4H, br), 4.53(2H, s), 8.36(1H, s), 8.40(1H, dd, J=8.6, 0.7), 8.64(1H, dd, J=8.6, 2.6), 9.53(1H, dd, J= 2.6, 0.7)

Example 242 Synthesis of Compound E-1

To a solution of 1-amino-(4-chlorobenzaldehyde)oxime (50 mg) in 4 ml of dichloromethane was added 40 mg of thiophosgene at 0° C. The mixture was stirred for 2 h at room temperature and water was added to the mixture. The resulting mixture was extracted with dichloromethane. The organic layer was extracted with aqueous potassium carbonate. The aqueous layer was neutralized by adding dilute hydrochloric acid and extracted with dichloromethane. The organic layer was dried and purified by the use of silica gel column chromatography to give 12 mg of 3-(4-chlorophenyl)-5-mercapto-1,2,4-oxadiazole.

¹H-NMR(CDCl₃): 6.96(2H, d, J=8.8 Hz), 7.32(2H, d, J=8.8 Hz).

Compound 10 (58 mg) was dissolved in 25% solution of hydrogen bromide in acetic acid (1 ml) and the mixture was stirred overnight at 40° C. The solvent was removed under reduced pressure and the residue was dissolved in 2 ml of DMF. The mixture was added to a solution of 35 mg of 3-(4-chlorophenyl)-5-mercapto-1,2,4-oxadiazole and 55 mg of potassium t-butoxide in 1 ml of DMF at ice-cooling. After stirring for 3 h at room temperature, water was added to the mixture. The resulting mixture was extracted with dichloromethane. The organic layer was washed with brine, dried, and purified by the use of preparative thin layer chromatography to give 12 mg of compound E-1. The physical data was shown in Table 28.

Example 243 Synthesis of Compound E-2

Compound E-2 was synthesized in a manner similar to that described in Example 242. The physical data was shown in Table 28.

Example 244 Synthesis of Compound E-3

To a solution of 2-amino-4′-chloroacetophenone hydrochloride (1.48 g) in 30 ml of dichloromethane were added 1.65 g of thiophosgene and 3.63 g of triethylamine at 0° C. and the mixture was stirred over night at room temperature. To the reaction mixture were added IN sodium hydroxide solution and methanol. The resulting mixture was stirred at room temperature and partitioned between ethyl acetate and water. The aqueous layer was neutralized by adding dil. hydrochloric acid and the resulting crystal was collected and dried to give 220 mg of 5-(4-chlorophenyl)-2-mercaptooxazole.

¹H-NMR(CDCl₃): 7.10(1H, s), 7.39(2H, d, J=8.6 Hz), 7.52(2H, d, J=8.6 Hz).

Condensation with pyrimidine derivative which was carried out in a manner similar to that described in Example 242 gave 284 mg of compound E-3. The physical data was shown in Table 28.

Example 245 Synthesis of Compound E-4

To a solution of 4-chlorobenzoic hydrazide (500 mg) in 10 ml of ethanol were added 444 mg of carbon disulfide and 163 mg of potassium hydroxide and the mixture was stirred for 2 h at room temperature. Ethanol was removed under reduced pressure and the obtained powder was gradually added to 3 ml of conc. sulfuric acid at ice-cooling. After stirring for 10 min, the mixture was poured into ice-water and extracted with ethyl acetate. The organic layer was extracted with aqueous potassium carbonate and the aqueous layer was neutralized by adding conc. hydrochloric acid. The precipitate was collected and dried to give 235 mg of 5-(4-chlorophenyl)-2-mercaptothiadiazole.

¹H-NMR(CDCl₃): 7.46(2H, d, J=8.5 Hz), 7.62(2f, d, J=8.5 Hz), 10.26(1H, br).

Condensation with pyrimidine derivative which was carried out in a manner similar to that described in Example 242 gave 301 mg of compound E-4. The physical data was shown in Table 28.

Example 246 Synthesis of Compound E-5

Isatoic anhydride (4.9 g) and thiosemicarbazide (2.8 g) were dissolved in 30 ml of DMF and the resulting mixture was stirred 20 h at 60 to 80° C. The solvent was removed under reduced pressure and the residue was recrystallized from methanol and ethanol to give 2.94 g of 1-(2-aminobenzoyl)thiosemicarbazide.

¹H-NMR(DMSOd6) 6.49(1H, t, J=7.8 Hz), 6.70(1H, dd, J=7.8, 1.3 Hz), 7.16(1H, dt, J=1.6, 7.8 Hz), 7.51(1H, br), 7.62(1H, d, J=7.8 Hz), 7.78(1H, br), 9.96(1H, br).

To a solution of 1-(2-aminobenzoyl)thiosemicarbazide (500 mg) and 2-ethoxyethanol was added 300 mg of potassium t-butoxide and the resulting mixture was heated at reflux for 2.5 h. The solvent was removed under reduced pressure and the residue was neutralized by adding aqueous potassium hydrogen sulfate. The resulting participate was collected to give 281 mg of 2-(2-aminophenyl)-5-mercaptotriazole.

¹H-NMR(DMSOd₆): 6.53(2H, br), 6.62(1H, t, J=7.8 Hz), 6.83(1H, d, J=7.8 Hz), 7.16(1H, dt, J=1.6, 7.8 Hz), 7.16(2H, br), 7.43(1H, dd, J=7.8, 1.6 Hz), 7.78(1H, br), 9.96(1H, br).

Condensation with pyrimidine derivative which was carried out in a manner similar to that described in Example 242 gave compound E-5. The physical data was shown in Table 28.

Example 247 Synthesis of Compound E-6

To a solution of ethyl 4-chlorobenzoylacetate (500 mg) in 4 ml of ethanol was added 202 mg of methylhydrazine and the resulting mixture was stirred over night at room temperature. The solvent was removed under reduced pressure and to the residue was purified by the use of silica gel column chromatography to give 199 mg of 3-(4-chlorophenyl)-1-methylpyrazoline-5-one.

¹H-NMR(CDCl₃): 3.41(3H, s), 3.58(2H, s), 7.39(2H, d, J=8.8 Hz), 7.60(2H, d, J=8.8Hz).

To a solution of the compound synthesized in the above step in dioxane was added 231 mg of Lawesson's Reagent and the resulting mixture was heated at reflux for 4 h. The reaction mixture was concentrated and the residue was purified by the use of silica gel column chromatography to give 91 mg of 3-(4-chlorophenyl)-1-methyl-5-mercaptopyrazole. 3-(4-chlorophenyl)-1-methyl-5-mercaptopyrazole (91 mg) and pyrimidine derivative are condensed in a manner similar to that described in Example 242 to give 103 mg of compound E-6. The physical data was shown in Table 28.

Example 248 Synthesis of Compound E 7

4-tolylboronic acid (500 mg), 2-bromofuran, and tetrakis(triphenylphosphine)palladium (177 mg) were added to the mixture of 24 ml of dimethoxyethane and 15 ml of ethanol under nitrogen atmosphere. Additionally 1N sodium carbonate (12 ml) was added to the mixture and the resulting mixture was heated at reflux for 2 h. Water was added to the mixture and the mitture was extracted with diethyl ether. The organic layer was dried and the solvent was removed under reduced pressure. The residue was purified by the use of silica gel column chromatography to give 438 mg of 2-(4-tolyl)furan.

¹H-NMR(CDCl₃): 2.36(3H, s), 6.45(1H, dd, J=3.4, 1.5 Hz), 6.59(11, d, J=3.4 Hz), 7.19(2H, d, J=8.0 Hz), 7.44(1H, d, J=1.5 Hz), 7.57(2, d, J=8.0 Hz).

To a solution of the compound obtained in the above step in 5 ml of THF was added 2.08 ml of 1.6 M butyllithium at −78° C. and the resulting mixture was stirred for 30 min. To the reaction mixture was added 133 mg of sulfur powder and the resulting mixture was stirred for an additional hour. Dil. hydrochloric acid was added to the mixture and the mixture was extracted with diethyl ether. The organic layer was washed with brine and the solvent was removed under reduced pressure. The residue was purified by the use of silica gel column chromatography gave 236 mg of 2-mercapto-5-(4-tolyl)furan.

¹H-NMR(CDCl₃): 2.38(3H, s), 6.66(1H, d, J=3.8 Hz), 6.72(11, d, J=3.8 Hz), 7.17 (2H, d, J=8.2 Hz), 7.58(1H, d, J=8.2 Hz).

2-mercapto-5-(4-tolyl)furan (70 mg) and pyrimidine derivative are condensed in a manner similar to that described in Example 242 to give 78 mg of compound E-7. The physical data was shown in Table 28.

TABLE 28

or

Example Compound No. No. R¹⁶ R¹⁸ Y ¹H-NMR (δ) ppm 242 E-1 Et 4-Cl

1.26(6H, t, J=7.5), 2.49(3H, s), 3.28(4H, br), 4.73(2H, s), 7.10(2H, d, J=8.8), 7.28(2H, d, J= 8.8), 8.13(1H, s) 243 E-2 Me H

1.30(3H, t, J=7.2), 2.48(3H, s), 2.98(3H, d, J= 3.41(2H, br), 4.50(2H, s), 7.46-7.50(3H, m), 8.06- 8.09(2H, m), 8.40(1H, s) 244 E-3 Et 4-Cl

1.30(6H, t, J=7.2), 2.47(3H, s), 3.37(4H, br), 4.38(2H, s), 7.28(1H, s), 7.35(2H, d, J=8.6), 7.48(2H, d, J=8.6), 8.27(1H, s) 245 E-4 Et 4-Cl

1.29(6H, t, J=7.2), 2.46(3H, s), 3.37(4H, br), 4.55(2H, s), 7.44(2H, d, J=8.5), 7.80(2H, d, J= 8.5), 8.23(1H, s) 246 E-5 Me 2-NH₂

1.36(3H, t, J=7.2), 2.52(3H, s), 3.10(3H, br), 3.47(2H, br), 4.31(2H, s), 5.49(2H, br), 6.71(1H, d, J=8.2), 6.72(1H, t, J=6.9), 7.13(1H, ddd, J=8.2, 6.9, 1.6), 7.97(1H, dd, J=6.9, 1.6), 8.43(1H, s) 247 E-6 Et 4-Cl

1.29(3H, t, J=7.1), 2.47(3H, s), 3.36(4H, br), 3.78(3H, s), 3.93(2H, s), 6.55(1H, s), 7.34(2H, d, J= 8.8), 7.66(2H, d, J=8.8), 7.85(1H, s) 248 E-7 Et 4-Me

1.28(6H, t, J=7.2), 2.36(3H, s), 2.46(3H, s), 3.34(4H, br), 3.96(2H, s), 6.39(1H, d, J=3.4), 6.51(1H, d, J=3.4), 7.17(2H, d, J=7.9), 7.54(2H, d, J=7.9), 7.78(1H, s)

Compounds F-1 to F-1142 shown in Tables 29 to 43 are able to synthesize in a manner similar to those described in Examples 1 to 248.

TABLE 29

or

Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-1  H H H 4-NH₂ F-2  H Me H 4-NH₂ F-3  H Et H 4-NH₂ F-4  H n-Pr H 4-NH₂ F-5  H i-Pr H 4-NH₂ F-6  H n-Bu H 4-NH₂ F-7  Me n-Pr H 4-NH₂ F-8  Me i-Pr H 4-NH₂ F-9  Me n-Bu H 4-NH₂ F-10 Et i-Pr H 4-NH₂ F-11 Et n-Bu H 4-NH₂ F-12 n-Pr n-Pr H 4-NH₂ F-13 n-Pr i-Pr H 4-NH₂ F-14 n-Pr n-Bu H 4-NH₂ F-15 i-Pr i-Pr H 4-NH₂ F-16 i-Pr n-Bu H 4-NH₂ F-17 n-Bu n-Bu H 4-NH₂ F-18 H H Me 4-NH₂ F-19 H Me Me 4-NH₂ F-20 H i-Pr Me 4-NH₂ F-21 H n-Bu Me 4-NH₂ F-22 Me n-Bu Me 4-NH₂ F-23 n-Pr i-Pr Me 4-NH₂ F-24 n-Pr n-Bu Me 4-NH₂ F-25 i-Pr n-Bu Me 4-NH₂ F-26 H H Et 4-NH₂ F-27 H Me Et 4-NH₂ F-28 H Et Et 4-NH₂ F-29 H n-Pr Et 4-NH₂ F-30 H n-Bu Et 4-NH₂ F-31 Me Et Et 4-NH₂ F-32 Me i-Pr Et 4-NH₂ F-33 Me n-Bu Et 4-NH₂ F-34 Et n-Pr Et 4-NH₂ F-35 Et i-Pr Et 4-NH₂ F-36 Et n-Bu Et 4-NH₂ F-37 n-Pr i-Pr Et 4-NH₂ F-38 n-Pr n-Bu Et 4-NH₂ F-39 i-Pr i-Pr Et 4-NH₂ F-40 i-Pr n-Bu Et 4-NH₂ F-41 n-Bu n-Bu Et 4-NH₂ F-42 H H H 4-NO₂ F-43 H Me H 4-NO₂ F-44 H Et H 4-NO₂ F-45 H n-Pr H 4-NO₂ F-46 H i-Pr H 4-NO₂ F-47 H n-Bu H 4-NO₂ F-48 Me n-Pr H 4-NO₂ F-49 Me i-Pr H 4-NO₂ F-50 Me n-Bu H 4-NO₂ F-51 Et i-Pr H 4-NO₂ F-52 Et n-Bu H 4-NO₂ F-53 n-Pr i-Pr H 4-NO₂ F-54 n-Pr n-Bu H 4-NO₂ F-55 i-Pr i-Pr H 4-NO₂ F-56 i-Pr n-Bu H 4-NO₂ F-57 n-Bu n-Bu H 4-NO₂ F-58 H H Me 4-NO₂ F-59 H Me Me 4-NO₂ F-60 H i-Pr Me 4-NO₂ F-61 H n-Bu Me 4-NO₂ F-62 Me n-Bu Me 4-NO₂ F-63 Et Et Me 4-NO₂ F-64 n-Pr i-Pr Me 4-NO₂ F-65 n-Pr n-Bu Me 4-NO₂ F-66 i-Pr n-Bu Me 4-NO₂ F-67 H H Et 4-NO₂ F-68 H Me Et 4-NO₂ F-69 H Et Et 4-NO₂ F-70 H n-Pr Et 4-NO₂ F-71 H i-Pr Et 4-NO₂ F-72 H n-Bu Et 4-NO₂ F-73 Me Et Et 4-NO₂ F-74 Me i-Pr Et 4-NO₂ F-75 Me n-Bu Et 4-NO₂ F-76 Et i-Pr Et 4-NO₂ F-77 Et n-Bu Et 4-NO₂ F-78 n-Pr i-Pr Et 4-NO₂ F-79 n-Pr n-Bu Et 4-NO₂ F-80 i-Pr i-Pr Et 4-NO₂

TABLE 30 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-81  i-Pr n-Bu Et 4-NO₂ F-82  n-Bu n-Bu Et 4-NO₂ F-83  H H H 2-F-4-NH₂ F-84  H Me H 2-F-4-NH₂ F-85  H Et H 2-F-4-NH₂ F-86  H n-Pr H 2-F-4-NH₂ F-87  H i-Pr H 2-F-4-NH₂ F-88  H n-Bu H 2-F-4-NH₂ F-89  Me Me H 2-F-4-NH₂ F-90  Me Et H 2-F-4-NH₂ F-91  Me n-Pr H 2-F-4-NH₂ F-92  Me i-Pr H 2-F-4-NH₂ F-93  Me n-Bu H 2-F-4-NH₂ F-94  Et Et H 2-F-4-NH₂ F-95  Et n-Pr H 2-F-4-NH₂ F-96  Et i-Pr H 2-F-4-NH₂ F-97  Et n-Bu H 2-F-4-NH₂ F-98  n-Pr n-Pr H 2-F-4-NH₂ F-99  n-Pr i-Pr H 2-F-4-NH₂ F-100 n-Pr n-Bu H 2-F-4-NH₂ F-101 i-Pr i-Pr H 2-F-4-NH₂ F-102 i-Pr n-Bu H 2-F-4-NH₂ F-103 n-Bu n-Bu H 2-F-4-NH₂ F-104 H H Me 2-F-4-NH₂ F-105 H Me Me 2-F-4-NH₂ F-106 H Et Me 2-F-4-NH₂ F-107 H n-Pr Me 2-F-4-NH₂ F-108 H i-Pr Me 2-F-4-NH₂ F-109 H n-Bu Me 2-F-4-NH₂ F-110 Me Me Me 2-F-4-NH₂ F-111 Me Et Me 2-F-4-NH₂ F-112 Me n-Pr Me 2-F-4-NH₂ F-113 Me i-Pr Me 2-F-4-NH₂ F-114 Me n-Bu Me 2-F-4-NH₂ F-115 Et n-Pr Me 2-F-4-NH₂ F-116 Et i-Pr Me 2-F-4-NH₂ F-117 Et n-Bu Me 2-F-4-NH₂ F-118 n-Pr n-Pr Me 2-F-4-NH₂ F-119 n-Pr i-Pr Me 2-F-4-NH₂ F-120 n-Pr n-Bu Me 2-F-4-NH₂ F-121 i-Pr i-Pr Me 2-F-4-NH₂ F-122 i-Pr n-Bu Me 2-F-4-NH₂ F-123 n-Bu n-Bu Me 2-F-4-NH₂ F-124 H H Et 2-F-4-NH₂ F-125 H Me Et 2-F-4-NH₂ F-126 H Et Et 2-F-4-NH₂ F-127 H n-Pr Et 2-F-4-NH₂ F-128 H i-Pr Et 2-F-4-NH₂ F-129 H n-Bu Et 2-F-4-NH₂ F-130 Me Me Et 2-F-4-NH₂ F-131 Me Et Et 2-F-4-NH₂ F-132 Me n-Pr Et 2-F-4-NH₂ F-133 Me i-Pr Et 2-F-4-NH₂ F-134 Me n-Bu Et 2-F-4-NH₂ F-135 Et Et Et 2-F-4-NH₂ F-136 Et n-Pr Et 2-F-4-NH₂ F-137 Et i-Pr Et 2-F-4-NH₂ F-138 Et n-Bu Et 2-F-4-NH₂ F-139 n-Pr n-Pr Et 2-F-4-NH₂ F-140 n-Pr i-Pr Et 2-F-4-NH₂ F-141 n-Pr n-Bu Et 2-F-4-NH₂ F-142 i-Pr i-Pr Et 2-F-4-NH₂ F-143 i-Pr n-Bu Et 2-F-4-NH₂ F-144 n-Bu n-Bu Et 2-F-4-NH₂ F-145 H H H 2-F-4-NO₂ F-146 H Me H 2-F-4-NO₂ F-147 H Et H 2-F-4-NO₂ F-148 H n-Pr H 2-F-4-NO₂ F-149 H i-Pr H 2-F-4-NO₂ F-150 H n-Bu H 2-F-4-NO₂ F-151 Me Me H 2-F-4-NO₂ F-152 Me Et H 2-F-4-NO₂ F-153 Me n-Pr H 2-F-4-NO₂ F-154 Me i-Pr H 2-F-4-NO₂ F-155 Me n-Bu H 2-F-4-NO₂ F-156 Et Et H 2-F-4-NO₂ F-157 Et n-Pr H 2-F-4-NO₂ F-158 Et i-Pr H 2-F-4-NO₂ F-159 Et n-Bu H 2-F-4-NO₂ F-160 n-Pr n-Pr H 2-F-4-NO₂

TABLE 31 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-161 n-Pr i-Pr H 2-F-4-NO₂ F-162 n-Pr n-Bu H 2-F-4-NO₂ F-163 i-Pr i-Pr H 2-F-4-NO₂ F-164 i-Pr n-Bu H 2-F-4-NO₂ F-165 n-Bu n-Bu H 2-F-4-NO₂ F-166 H H Me 2-F-4-NO₂ F-167 H Me Me 2-F-4-NO₂ F-168 H Et Me 2-F-4-NO₂ F-169 H n-Pr Me 2-F-4-NO₂ F-170 H i-Pr Me 2-F-4-NO₂ F-171 H n-Bu Me 2-F-4-NO₂ F-172 Me Me Me 2-F-4-NO₂ F-173 Me Et Me 2-F-4-NO₂ F-174 Me n-Pr Me 2-F-4-NO₂ F-175 Me i-Pr Me 2-F-4-NO₂ F-176 Me n-Bu Me 2-F-4-NO₂ F-177 Et n-Pr Me 2-F-4-NO₂ F-178 Et i-Pr Me 2-F-4-NO₂ F-179 Et n-Bu Me 2-F-4-NO₂ F-180 n-Pr n-Pr Me 2-F-4-NO₂ F-181 n-Pr i-Pr Me 2-F-4-NO₂ F-182 n-Pr n-Bu Me 2-F-4-NO₂ F-183 i-Pr i-Pr Me 2-F-4-NO₂ F-184 i-Pr n-Bu Me 2-F-4-NO₂ F-185 n-Bu n-Bu Me 2-F-4-NO₂ F-186 H H Et 2-F-4-NO₂ F-187 H Me Et 2-F-4-NO₂ F-188 H Et Et 2-F-4-NO₂ F-189 H n-Pr Et 2-F-4-NO₂ F-190 H i-Pr Et 2-F-4-NO₂ F-191 H n-Bu Et 2-F-4-NO₂ F-192 Me Me Et 2-F-4-NO₂ F-193 Me Et Et 2-F-4-NO₂ F-194 Me n-Pr Et 2-F-4-NO₂ F-195 Me i-Pr Et 2-F-4-NO₂ F-196 Me n-Bu Et 2-F-4-NO₂ F-197 Et Et Et 2-F-4-NO₂ F-198 Et n-Pr Et 2-F-4-NO₂ F-199 Et i-Pr Et 2-F-4-NO₂ F-200 Et n-Bu Et 2-F-4-NO₂ F-201 n-Pr n-Pr Et 2-F-4-NO₂ F-202 n-Pr i-Pr Et 2-F-4-NO₂ F-203 n-Pr n-Bu Et 2-F-4-NO₂ F-204 i-Pr i-Pr Et 2-F-4-NO₂ F-205 i-Pr n-Bu Et 2-F-4-NO₂ F-206 n-Bu n-Bu Et 2-F-4-NO₂ F-207 H H H 2-OMe-4-NH₂ F-208 H Me H 2-OMe-4-NH₂ F-209 H Et H 2-OMe-4-NH₂ F-210 H n-Pr H 2-OMe-4-NH₂ F-211 H i-Pr H 2-OMe-4-NH₂ F-212 H n-Bu H 2-OMe-4-NH₂ F-213 Me Me H 2-OMe-4-NH₂ F-214 Me Et H 2-OMe-4-NH₂ F-215 Me n-Pr H 2-OMe-4-NH₂ F-216 Me i-Pr H 2-OMe-4-NH₂ F-217 Me n-Bu H 2-OMe-4-NH₂ F-218 Et Et H 2-OMe-4-NH₂ F-219 Et n-Pr H 2-OMe-4-NH₂ F-220 Et i-Pr H 2-OMe-4-NH₂ F-221 Et n-Bu H 2-OMe-4-NH₂ F-222 n-Pr n-Pr H 2-OMe-4-NH₂ F-223 n-Pr i-Pr H 2-OMe-4-NH₂ F-224 n-Pr n-Bu H 2-OMe-4-NH₂ F-225 i-Pr i-Pr H 2-OMe-4-NH₂ F-226 i-Pr n-Bu H 2-OMe-4-NH₂ F-227 n-Bu n-Bu H 2-OMe-4-NH₂ F-228 H H Me 2-OMe-4-NH₂ F-229 H Me Me 2-OMe-4-NH₂ F-230 H Et Me 2-OMe-4-NH₂ F-231 H n-Pr Me 2-OMe-4-NH₂ F-232 H i-Pr Me 2-OMe-4-NH₂ F-233 H n-Bu Me 2-OMe-4-NH₂ F-234 Me Me Me 2-OMe-4-NH₂ F-235 Me Et Me 2-OMe-4-NH₂ F-236 Me n-Pr Me 2-OMe-4-NH₂ F-237 Me i-Pr Me 2-OMe-4-NH₂ F-238 Me n-Bu Me 2-OMe-4-NH₂ F-239 Et n-Pr Me 2-OMe-4-NH₂ F-240 Et i-Pr Me 2-OMe-4-NH₂

TABLE 32 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-241 Et n-Bu Me 2-OMe-4-NH₂ F-242 n-Pr i-Pr Me 2-OMe-4-NH₂ F-243 n-Pr n-Bu Me 2-OMe-4-NH₂ F-244 i-Pr i-Pr Me 2-OMe-4-NH₂ F-245 i-Pr n-Bu Me 2-OMe-4-NH₂ F-246 n-Bu n-Bu Me 2-OMe-4-NH₂ F-247 H H Et 2-OMe-4-NH₂ F-248 H Me Et 2-OMe-4-NH₂ F-249 H Et Et 2-OMe-4-NH₂ F-250 H n-Pr Et 2-OMe-4-NH₂ F-251 H i-Pr Et 2-OMe-4-NH₂ F-252 H n-Bu Et 2-OMe-4-NH₂ F-253 Me Me Et 2-OMe-4-NH₂ F-254 Me Et Et 2-OMe-4-NH₂ F-255 Me n-Pr Et 2-OMe-4-NH₂ F-256 Me i-Pr Et 2-OMe-4-NH₂ F-257 Me n-Bu Et 2-OMe-4-NH₂ F-258 Et Et Et 2-OMe-4-NH₂ F-259 Et n-Pr Et 2-OMe-4-NH₂ F-260 Et i-Pr Et 2-OMe-4-NH₂ F-261 Et n-Bu Et 2-OMe-4-NH₂ F-262 n-Pr n-Pr Et 2-OMe-4-NH₂ F-263 n-Pr i-Pr Et 2-OMe-4-NH₂ F-264 n-Pr n-Bu Et 2-OMe-4-NH₂ F-265 i-Pr i-Pr Et 2-OMe-4-NH₂ F-266 i-Pr n-Bu Et 2-OMe-4-NH₂ F-267 n-Bu n-Bu Et 2-OMe-4-NH₂ F-268 H H H 2-OMe-4-NO₂ F-269 H Me H 2-OMe-4-NO₂ F-270 H Et H 2-OMe-4-NO₂ F-271 H n-Pr H 2-OMe-4-NO₂ F-272 H i-Pr H 2-OMe-4-NO₂ F-273 H n-Bu H 2-OMe-4-NO₂ F-274 Me Me H 2-OMe-4-NO₂ F-275 Me Et H 2-OMe-4-NO₂ F-276 Me n-Pr H 2-OMe-4-NO₂ F-277 Me i-Pr H 2-OMe-4-NO₂ F-278 Me n-Bu H 2-OMe-4-NO₂ F-279 Et n-Pr H 2-OMe-4-NO₂ F-280 Et i-Pr H 2-OMe-4-NO₂ F-281 Et n-Bu H 2-OMe-4-NO₂ F-282 n-Pr n-Pr H 2-OMe-4-NO₂ F-283 n-Pr i-Pr H 2-OMe-4-NO₂ F-284 n-Pr n-Bu H 2-OMe-4-NO₂ F-285 i-Pr i-Pr H 2-OMe-4-NO₂ F-286 i-Pr n-Bu H 2-OMe-4-NO₂ F-287 n-Bu n-Bu H 2-OMe-4-NO₂ F-288 H H Me 2-OMe-4-NO₂ F-289 H Me Me 2-OMe-4-NO₂ F-290 H Et Me 2-OMe-4-NO₂ F-291 H n-Pr Me 2-OMe-4-NO₂ F-292 H i-Pr Me 2-OMe-4-NO₂ F-293 H n-Bu Me 2-OMe-4-NO₂ F-294 Me Et Me 2-OMe-4-NO₂ F-295 Me n-Pr Me 2-OMe-4-NO₂ F-296 Me i-Pr Me 2-OMe-4-NO₂ F-297 Me n-Bu Me 2-OMe-4-NO₂ F-298 Et n-Pr Me 2-OMe-4-NO₂ F-299 Et i-Pr Me 2-OMe-4-NO₂ F-300 Et n-Bu Me 2-OMe-4-NO₂ F-301 n-Pr n-Pr Me 2-OMe-4-NO₂ F-302 n-Pr i-Pr Me 2-OMe-4-NO₂ F-303 n-Pr n-Bu Me 2-OMe-4-NO₂ F-304 i-Pr i-Pr Me 2-OMe-4-NO₂ F-305 i-Pr n-Bu Me 2-OMe-4-NO₂ F-306 n-Bu n-Bu Me 2-OMe-4-NO₂ F-307 H H Et 2-OMe-4-NO₂ F-308 H Me Et 2-OMe-4-NO₂ F-309 H Et Et 2-OMe-4-NO₂ F-310 H n-Pr Et 2-OMe-4-NO₂ F-311 H i-Pr Et 2-OMe-4-NO₂ F-312 H n-Bu Et 2-OMe-4-NO₂ F-313 Me Me Et 2-OMe-4-NO₂ F-314 Me Et Et 2-OMe-4-NO₂ F-315 Me n-Pr Et 2-OMe-4-NO₂ F-316 Me i-Pr Et 2-OMe-4-NO₂ F-317 Me n-Bu Et 2-OMe-4-NO₂ F-318 Et Et Et 2-OMe-4-NO₂ F-319 Et n-Pr Et 2-OMe-4-NO₂ F-320 Et i-Pr Et 2-OMe-4-NO₂

TABLE 33 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-321 Et n-Bu Et 2-OMe-4-NO₂ F-322 n-Pr n-Pr Et 2-OMe-4-NO₂ F-323 n-Pr i-Pr Et 2-OMe-4-NO₂ F-324 n-Pr n-Bu Et 2-OMe-4-NO₂ F-325 i-Pr i-Pr Et 2-OMe-4-NO₂ F-326 i-Pr n-Bu Et 2-OMe-4-NO₂ F-327 n-Bu n-Bu Et 2-OMe-4-NO₂ F-328 H H H 2-NH₂-4-F F-329 H Me H 2-NH₂-4-F F-330 H Et H 2-NH₂-4-F F-331 H n-Pr H 2-NH₂-4-F F-332 H i-Pr H 2-NH₂-4-F F-333 H n-Bu H 2-NH₂-4-F F-334 Me Me H 2-NH₂-4-F F-335 Me Et H 2-NH₂-4-F F-336 Me n-Pr H 2-NH₂-4-F F-337 Me i-Pr H 2-NH₂-4-F F-338 Me n-Bu H 2-NH₂-4-F F-339 Et n-Pr H 2-NH₂-4-F F-340 Et i-Pr H 2-NH₂-4-F F-341 Et n-Bu H 2-NH₂-4-F F-342 n-Pr n-Pr H 2-NH₂-4-F F-343 n-Pr i-Pr H 2-NH₂-4-F F-344 n-Pr n-Bu H 2-NH₂-4-F F-345 i-Pr i-Pr H 2-NH₂-4-F F-346 i-Pr n-Bu H 2-NH₂-4-F F-347 n-Bu n-Bu H 2-NH₂-4-F F-348 H H Me 2-NH₂-4-F F-349 H Me Me 2-NH₂-4-F F-350 H Et Me 2-NH₂-4-F F-351 H n-Pr Me 2-NH₂-4-F F-352 H i-Pr Me 2-NH₂-4-F F-353 H n-Bu Me 2-NH₂-4-F F-354 Me Me Me 2-NH₂-4-F F-355 Me Et Me 2-NH₂-4-F F-356 Me n-Pr Me 2-NH₂-4-F F-357 Me i-Pr Me 2-NH₂-4-F F-358 Me n-Bu Me 2-NH₂-4-F F-359 Et n-Pr Me 2-NH₂-4-F F-360 Et i-Pr Me 2-NH₂-4-F F-361 Et n-Bu Me 2-NH₂-4-F F-362 n-Pr n-Pr Me 2-NH₂-4-F F-363 n-Pr i-Pr Me 2-NH₂-4-F F-364 n-Pr n-Bu Me 2-NH₂-4-F F-365 i-Pr i-Pr Me 2-NH₂-4-F F-366 i-Pr n-Bu Me 2-NH₂-4-F F-367 n-Bu n-Bu Me 2-NH₂-4-F F-368 H H Et 2-NH₂-4-F F-369 H Me Et 2-NH₂-4-F F-370 H Et Et 2-NH₂-4-F F-371 H n-Pr Et 2-NH₂-4-F F-372 H i-Pr Et 2-NH₂-4-F F-373 H n-Bu Et 2-NH₂-4-F F-374 Me Me Et 2-NH₂-4-F F-375 Me Et Et 2-NH₂-4-F F-376 Me n-Pr Et 2-NH₂-4-F F-377 Me i-Pr Et 2-NH₂-4-F F-378 Me n-Bu Et 2-NH₂-4-F F-379 Et Et Et 2-NH₂-4-F F-380 Et n-Pr Et 2-NH₂-4-F F-381 Et i-Pr Et 2-NH₂-4-F F-382 Et n-Bu Et 2-NH₂-4-F F-383 n-Pr i-Pr Et 2-NH₂-4-F F-384 n-Pr n-Bu Et 2-NH₂-4-F F-385 i-Pr i-Pr Et 2-NH₂-4-F F-386 i-Pr n-Bu Et 2-NH₂-4-F F-387 n-Bu n-Bu Et 2-NH₂-4-F F-388 H H H 2-NO₂-4-F F-389 H Me H 2-NO₂-4-F F-390 H Et H 2-NO₂-4-F F-391 H n-Pr H 2-NO₂-4-F F-392 H i-Pr H 2-NO₂-4-F F-393 H n-Bu H 2-NO₂-4-F F-394 Me Me H 2-NO₂-4-F F-395 Me Et H 2-NO₂-4-F F-396 Me n-Pr H 2-NO₂-4-F F-397 Me i-Pr H 2-NO₂-4-F F-398 Me n-Bu H 2-NO₂-4-F F-399 Et Et H 2-NO₂-4-F F-400 Et n-Pr H 2-NO₂-4-F

TABLE 34 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-401 Et i-Pr H 2-NO₂-4-F F-402 Et n-Bu H 2-NO₂-4-F F-403 n-Pr n-Pr H 2-NO₂-4-F F-404 n-Pr i-Pr H 2-NO₂-4-F F-405 n-Pr n-Bu H 2-NO₂-4-F F-406 i-Pr i-Pr H 2-NO₂-4-F F-407 i-Pr n-Bu H 2-NO₂-4-F F-408 n-Bu n-Bu H 2-NO₂-4-F F-409 H H Me 2-NO₂-4-F F-410 H Me Me 2-NO₂-4-F F-411 H Et Me 2-NO₂-4-F F-412 H n-Pr Me 2-NO₂-4-F F-413 H i-Pr Me 2-NO₂-4-F F-414 H n-Bu Me 2-NO₂-4-F F-415 Me Me Me 2-NO₂-4-F F-416 Me Et Me 2-NO₂-4-F F-417 Me n-Pr Me 2-NO₂-4-F F-418 Me i-Pr Me 2-NO₂-4-F F-419 Me n-Bu Me 2-NO₂-4-F F-420 Et Et Me 2-NO₂-4-F F-421 Et n-Pr Me 2-NO₂-4-F F-422 Et i-Pr Me 2-NO₂-4-F F-423 Et n-Bu Me 2-NO₂-4-F F-424 n-Pr n-Pr Me 2-NO₂-4-F F-425 n-Pr i-Pr Me 2-NO₂-4-F F-426 n-Pr n-Bu Me 2-NO₂-4-F F-427 i-Pr i-Pr Me 2-NO₂-4-F F-428 i-Pr n-Bu Me 2-NO₂-4-F F-429 n-Bu n-Bu Me 2-NO₂-4-F F-430 H H Et 2-NO₂-4-F F-431 H Me Et 2-NO₂-4-F F-432 H Et Et 2-NO₂-4-F F-433 H n-Pr Et 2-NO₂-4-F F-434 H i-Pr Et 2-NO₂-4-F F-435 H n-Bu Et 2-NO₂-4-F F-436 Me Me Et 2-NO₂-4-F F-437 Me Et Et 2-NO₂-4-F F-438 Me n-Pr Et 2-NO₂-4-F F-439 Me i-Pr Et 2-NO₂-4-F F-440 Me n-Bu Et 2-NO₂-4-F F-441 Et Et Et 2-NO₂-4-F F-442 Et n-Pr Et 2-NO₂-4-F F-443 Et i-Pr Et 2-NO₂-4-F F-444 Et n-Bu Et 2-NO₂-4-F F-445 n-Pr n-Pr Et 2-NO₂-4-F F-446 n-Pr i-Pr Et 2-NO₂-4-F F-447 n-Pr n-Bu Et 2-NO₂-4-F F-448 i-Pr i-Pr Et 2-NO₂-4-F F-449 i-Pr n-Bu Et 2-NO₂-4-F F-450 n-Bu n-Bu Et 2-NO₂-4-F F-451 H Et H 2-Cl-4-NH₂ F-452 Me Me H 2-Cl-4-NH₂ F-453 Me Et H 2-Cl-4-NH₂ F-454 Me n-Pr H 2-Cl-4-NH₂ F-455 Me i-Pr H 2-Cl-4-NH₂ F-456 Me n-Bu H 2-Cl-4-NH₂ F-457 Et Et H 2-Cl-4-NH₂ F-458 Et n-Pr H 2-Cl-4-NH₂ F-459 Et i-Pr H 2-Cl-4-NH₂ F-460 n-Pr n-Pr H 2-Cl-4-NH₂ F-461 n-Pr i-Pr H 2-Cl-4-NH₂ F-462 i-Pr i-Pr H 2-Cl-4-NH₂ F-463 H Et Me 2-Cl-4-NH₂ F-464 Me Me Me 2-Cl-4-NH₂ F-465 Me Et Me 2-Cl-4-NH₂ F-466 Me n-Pr Me 2-Cl-4-NH₂ F-467 Me i-Pr Me 2-Cl-4-NH₂ F-468 Me n-Bu Me 2-Cl-4-NH₂ F-469 Et n-Pr Me 2-Cl-4-NH₂ F-470 Et i-Pr Me 2-Cl-4-NH₂ F-471 n-Pr n-Pr Me 2-Cl-4-NH₂ F-472 n-Pr i-Pr Me 2-Cl-4-NH₂ F-473 i-Pr i-Pr Me 2-Cl-4-NH₂ F-474 H Et Et 2-Cl-4-NH₂ F-475 Me Me Et 2-Cl-4-NH₂ F-476 Me Et Et 2-Cl-4-NH₂ F-477 Me n-Pr Et 2-Cl-4-NH₂ F-478 Me i-Pr Et 2-Cl-4-NH₂ F-479 Me n-Bu Et 2-Cl-4-NH₂ F-480 Et Et Et 2-Cl-4-NH₂

TABLE 35 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-481 Et n-Pr Et 2-Cl-4-NH₂ F-482 Et i-Pr Et 2-Cl-4-NH₂ F-483 H Et H 2-Me-4-NH₂ F-484 Me Me H 2-Me-4-NH₂ F-485 Me Et H 2-Me-4-NH₂ F-486 Me n-Pr H 2-Me-4-NH₂ F-487 Me i-Pr H 2-Me-4-NH₂ F-488 Me n-Bu H 2-Me-4-NH₂ F-489 Et Et H 2-Me-4-NH₂ F-490 Et n-Pr H 2-Me-4-NH₂ F-491 Et i-Pr H 2-Me-4-NH₂ F-492 n-Pr n-Pr H 2-Me-4-NH₂ F-493 n-Pr i-Pr H 2-Me-4-NH₂ F-494 i-Pr i-Pr H 2-Me-4-NH₂ F-495 H Et Me 2-Me-4-NH₂ F-496 Me Me Me 2-Me-4-NH₂ F-497 Me Et Me 2-Me-4-NH₂ F-498 Me n-Pr Me 2-Me-4-NH₂ F-499 Me i-Pr Me 2-Me-4-NH₂ F-500 Me n-Bu Me 2-Me-4-NH₂ F-501 Et Et Me 2-Me-4-NH₂ F-502 Et n-Pr Me 2-Me-4-NH₂ F-503 Et i-Pr Me 2-Me-4-NH₂ F-504 n-Pr n-Pr Me 2-Me-4-NH₂ F-505 n-Pr i-Pr Me 2-Me-4-NH₂ F-506 i-Pr i-Pr Me 2-Me-4-NH₂ F-507 H Et Et 2-Me-4-NH₂ F-508 Me Me Et 2-Me-4-NH₂ F-509 Me Et Et 2-Me-4-NH₂ F-510 Me n-Pr Et 2-Me-4-NH₂ F-511 Me i-Pr Et 2-Me-4-NH₂ F-512 Me n-Bu Et 2-Me-4-NH₂ F-513 Et Et Et 2-Me-4-NH₂ F-514 Et n-Pr Et 2-Me-4-NH₂ F-515 Et i-Pr Et 2-Me-4-NH₂ F-516 H Et H 2-CF₃-4-NH₂ F-517 Me Me H 2-CF₃-4-NH₂ F-518 Me Et H 2-CF₃-4-NH₂ F-519 Me n-Pr H 2-CF₃-4-NH₂ F-520 Me i-Pr H 2-CF₃-4-NH₂ F-521 Me n-Bu H 2-CF₃-4-NH₂ F-522 Et Et H 2-CF₃-4-NH₂ F-523 Et n-Pr H 2-CF₃-4-NH₂ F-524 Et i-Pr H 2-CF₃-4-NH₂ F-525 n-Pr n-Pr H 2-CF₃-4-NH₂ F-526 n-Pr i-Pr H 2-CF₃-4-NH₂ F-527 i-Pr i-Pr H 2-CF₃-4-NH₂ F-528 H Et Me 2-CF₃-4-NH₂ F-529 Me Me Me 2-CF₃-4-NH₂ F-530 Me Et Me 2-CF₃-4-NH₂ F-531 Me n-Pr Me 2-CF₃-4-NH₂ F-532 Me i-Pr Me 2-CF₃-4-NH₂ F-533 Me n-Bu Me 2-CF₃-4-NH₂ F-534 Et Et Me 2-CF₃-4-NH₂ F-535 Et n-Pr Me 2-CF₃-4-NH₂ F-536 Et i-Pr Me 2-CF₃-4-NH₂ F-537 n-Pr n-Pr Me 2-CF₃-4-NH₂ F-538 n-Pr i-Pr Me 2-CF₃-4-NH₂ F-539 i-Pr i-Pr Me 2-CF₃-4-NH₂ F-540 Me Et Et 2-CF₃-4-NH₂ F-541 Me n-Pr Et 2-CF₃-4-NH₂ F-542 Me i-Pr Et 2-CF₃-4-NH₂ F-543 Me n-Bu Et 2-CF₃-4-NH₂ F-544 Me i-Pr Et 2-CF₃-4-NH₂ F-545 Me n-Bu Et 2-CF₃-4-NH₂ F-546 Et Et Et 2-CF₃-4-NH₂ F-547 Et n-Pr Et 2-CF₃-4-NH₂ F-548 Et i-Pr Et 2-CF₃-4-NH₂ F-549 H Et H 2-OEt-4-NH₂ F-550 Me Me H 2-OEt-4-NH₂ F-551 Me Et H 2-OEt-4-NH₂ F-552 Me n-Pr H 2-OEt-4-NH₂ F-553 Me i-Pr H 2-OEt-4-NH₂ F-554 Me n-Bu H 2-OEt-4-NH₂ F-555 Et Et H 2-OEt-4-NH₂ F-556 Et n-Pr H 2-OEt-4-NH₂ F-557 Et i-Pr H 2-OEt-4-NH₂ F-558 n-Pr n-Pr H 2-OEt-4-NH₂ F-559 n-Pr i-Pr H 2-OEt-4-NH₂ F-560 i-Pr i-Pr H 2-OEt-4-NH₂

TABLE 36 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-561 H Et Me 2-OEt-4-NH₂ F-562 Me Me Me 2-OEt-4-NH₂ F-563 Me Et Me 2-OEt-4-NH₂ F-564 Me n-Pr Me 2-OEt-4-NH₂ F-565 Me i-Pr Me 2-OEt-4-NH₂ F-566 Me n-Bu Me 2-OEt-4-NH₂ F-567 Et Et Me 2-OEt-4-NH₂ F-568 Et n-Pr Me 2-OEt-4-NH₂ F-569 Et i-Pr Me 2-OEt-4-NH₂ F-570 n-Pr n-Pr Me 2-OEt-4-NH₂ F-571 n-Pr i-Pr Me 2-OEt-4-NH₂ F-572 i-Pr i-Pr Me 2-OEt-4-NH₂ F-573 H Et Et 2-OEt-4-NH₂ F-574 Me Me Et 2-OEt-4-NH₂ F-575 Me Et Et 2-OEt-4-NH₂ F-576 Me n-Pr Et 2-OEt-4-NH₂ F-577 Me i-Pr Et 2-OEt-4-NH₂ F-578 Me n-Bu Et 2-OEt-4-NH₂ F-579 Et Et Et 2-OEt-4-NH₂ F-580 Et n-Pr Et 2-OEt-4-NH₂ F-581 Et i-Pr Et 2-OEt-4-NH₂ F-582 H Et H 2-OCF₃-4-NH₂ F-583 Me Me H 2-OCF₃-4-NH₂ F-584 Me Et H 2-OCF₃-4-NH₂ F-585 Me n-Pr H 2-OCF₃-4-NH₂ F-586 Me i-Pr H 2-OCF₃-4-NH₂ F-587 Me n-Bu H 2-OCF₃-4-NH₂ F-588 Et Et H 2-OCF₃-4-NH₂ F-589 Et n-Pr H 2-OCF₃-4-NH₂ F-590 Et i-Pr H 2-OCF₃-4-NH₂ F-591 n-Pr n-Pr H 2-OCF₃-4-NH₂ F-592 n-Pr i-Pr H 2-OCF₃-4-NH₂ F-593 i-Pr i-Pr H 2-OCF₃-4-NH₂ F-594 H Et Me 2-OCF₃-4-NH₂ F-595 Me Me Me 2-OCF₃-4-NH₂ F-596 Me Et Me 2-OCF₃-4-NH₂ F-597 Me n-Pr Me 2-OCF₃-4-NH₂ F-598 Me i-Pr Me 2-OCF₃-4-NH₂ F-599 Me n-Bu Me 2-OCF₃-4-NH₂ F-600 Et Et Me 2-OCF₃-4-NH₂ F-601 Et n-Pr Me 2-OCF₃-4-NH₂ F-602 Et i-Pr Me 2-OCF₃-4-NH₂ F-603 n-Pr n-Pr Me 2-OCF₃-4-NH₂ F-604 n-Pr i-Pr Me 2-OCF₃-4-NH₂ F-605 i-Pr i-Pr Me 2-OCF₃-4-NH₂ F-606 H Et Et 2-OCF₃-4-NH₂ F-607 Me Me Et 2-OCF₃-4-NH₂ F-608 Me Et Et 2-OCF₃-4-NH₂ F-609 Me n-Pr Et 2-OCF₃-4-NH₂ F-610 Me i-Pr Et 2-OCF₃-4-NH₂ F-611 Me n-Bu Et 2-OCF₃-4-NH₂ F-612 Et Et Et 2-OCF₃-4-NH₂ F-613 Et n-Pr Et 2-OCF₃-4-NH₂ F-614 Et i-Pr Et 2-OCF₃-4-NH₂ F-615 H Et H 2-Cl-4-NO₂ F-616 Me Me H 2-Cl-4-NO₂ F-617 Me Et H 2-Cl-4-NO₂ F-618 Me n-Pr H 2-Cl-4-NO₂ F-619 Me i-Pr H 2-Cl-4-NO₂ F-620 Me n-Bu H 2-Cl-4-NO₂ F-621 Et Et H 2-Cl-4-NO₂ F-622 Et n-Pr H 2-Cl-4-NO₂ F-623 Et i-Pr H 2-Cl-4-NO₂ F-624 n-Pr n-Pr H 2-Cl-4-NO₂ F-625 n-Pr i-Pr H 2-Cl-4-NO₂ F-626 i-Pr i-Pr H 2-Cl-4-NO₂ F-627 H Et Me 2-Cl-4-NO₂ F-628 Me Me Me 2-Cl-4-NO₂ F-629 Me Et Me 2-Cl-4-NO₂ F-630 Me n-Pr Me 2-Cl-4-NO₂ F-631 Me i-Pr Me 2-Cl-4-NO₂ F-632 Me n-Bu Me 2-Cl-4-NO₂ F-633 Et Et Me 2-Cl-4-NO₂ F-634 Et n-Pr Me 2-Cl-4-NO₂ F-635 Et i-Pr Me 2-Cl-4-NO₂ F-636 n-Pr n-Pr Me 2-Cl-4-NO₂ F-637 n-Pr i-Pr Me 2-Cl-4-NO₂ F-638 i-Pr i-Pr Me 2-Cl-4-NO₂ F-639 H Et Et 2-Cl-4-NO₂ F-640 Me Me Et 2-Cl-4-NO₂

TABLE 37 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-641 Me Et Et 2-Cl-4-NO₂ F-642 Me n-Pr Et 2-Cl-4-NO₂ F-643 Me i-Pr Et 2-Cl-4-NO₂ F-644 Me n-Bu Et 2-Cl-4-NO₂ F-645 Et Et Et 2-Cl-4-NO₂ F-646 Et n-Pr Et 2-Cl-4-NO₂ F-647 Et i-Pr Et 2-Cl-4-NO₂ F-648 H Et H 2-Me-4-NO₂ F-649 Me Me H 2-Me-4-NO₂ F-650 Me Et H 2-Me-4-NO₂ F-651 Me n-Pr H 2-Me-4-NO₂ F-652 Me i-Pr H 2-Me-4-NO₂ F-653 Me n-Bu H 2-Me-4-NO₂ F-654 Et Et H 2-Me-4-NO₂ F-655 Et n-Pr H 2-Me-4-NO₂ F-656 Et i-Pr H 2-Me-4-NO₂ F-657 n-Pr n-Pr H 2-Me-4-NO₂ F-658 n-Pr i-Pr H 2-Me-4-NO₂ F-659 i-Pr i-Pr H 2-Me-4-NO₂ F-660 H Et Me 2-Me-4-NO₂ F-661 Me Me Me 2-Me-4-NO₂ F-662 Me Et Me 2-Me-4-NO₂ F-663 Me n-Pr Me 2-Me-4-NO₂ F-664 Me i-Pr Me 2-Me-4-NO₂ F-665 Me n-Bu Me 2-Me-4-NO₂ F-666 Et Et Me 2-Me-4-NO₂ F-667 Et n-Pr Me 2-Me-4-NO₂ F-668 Et i-Pr Me 2-Me-4-NO₂ F-669 n-Pr n-Pr Me 2-Me-4-NO₂ F-670 n-Pr i-Pr Me 2-Me-4-NO₂ F-671 i-Pr i-Pr Me 2-Me-4-NO₂ F-672 H Et Et 2-Me-4-NO₂ F-673 Me Me Et 2-Me-4-NO₂ F-674 Me Et Et 2-Me-4-NO₂ F-675 Me n-Pr Et 2-Me-4-NO₂ F-676 Me i-Pr Et 2-Me-4-NO₂ F-677 Me n-Bu Et 2-Me-4-NO₂ F-678 Et Et Et 2-Me-4-NO₂ F-679 Et n-Pr Et 2-Me-4-NO₂ F-680 Et i-Pr Et 2-Me-4-NO₂ F-681 H Et H 2-OEt-4-NO₂ F-682 Me Me H 2-OEt-4-NO₂ F-683 Me Et H 2-OEt-4-NO₂ F-684 Me n-Pr H 2-OEt-4-NO₂ F-685 Me i-Pr H 2-OEt-4-NO₂ F-686 Me n-Bu H 2-OEt-4-NO₂ F-687 Et Et H 2-OEt-4-NO₂ F-688 Et n-Pr H 2-OEt-4-NO₂ F-689 Et i-Pr H 2-OEt-4-NO₂ F-690 n-Pr n-Pr H 2-OEt-4-NO₂ F-691 n-Pr i-Pr H 2-OEt-4-NO₂ F-692 i-Pr i-Pr H 2-OEt-4-NO₂ F-693 H Et Me 2-OEt-4-NO₂ F-694 Me Me Me 2-OEt-4-NO₂ F-695 Me Et Me 2-OEt-4-NO₂ F-696 Me n-Pr Me 2-OEt-4-NO₂ F-697 Me i-Pr Me 2-OEt-4-NO₂ F-698 Me n-Bu Me 2-OEt-4-NO₂ F-699 Et Et Me 2-OEt-4-NO₂ F-700 Et n-Pr Me 2-OEt-4-NO₂ F-701 Et i-Pr Me 2-OEt-4-NO₂ F-702 n-Pr n-Pr Me 2-OEt-4-NO₂ F-703 n-Pr i-Pr Me 2-OEt-4-NO₂ F-704 i-Pr i-Pr Me 2-OEt-4-NO₂ F-705 H Et Et 2-OEt-4-NO₂ F-706 Me Me Et 2-OEt-4-NO₂ F-707 Me Et Et 2-OEt-4-NO₂ F-708 Me n-Pr Et 2-OEt-4-NO₂ F-709 Me i-Pr Et 2-OEt-4-NO₂ F-710 Me n-Bu Et 2-OEt-4-NO₂ F-711 Et Et Et 2-OEt-4-NO₂ F-712 Et n-Pr Et 2-OEt-4-NO₂ F-713 Et i-Pr Et 2-OEt-4-NO₂ F-714 H Et H 2-OCF₃-4-NO₂ F-715 Me Me H 2-OCF₃-4-NO₂ F-716 Me Et H 2-OCF₃-4-NO₂ F-717 Me n-Pr H 2-OCF₃-4-NO₂ F-718 Me i-Pr H 2-OCF₃-4-NO₂ F-719 Me n-Bu H 2-OCF₃-4-NO₂ F-720 Et Et H 2-OCF₃-4-NO₂

TABLE 38 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-721 Et n-Pr H 2-OCF₃-4-NO₂ F-722 Et i-Pr H 2-OCF₃-4-NO₂ F-723 n-Pr n-Pr H 2-OCF₃-4-NO₂ F-724 n-Pr i-Pr H 2-OCF₃-4-NO₂ F-725 i-Pr i-Pr H 2-OCF₃-4-NO₂ F-726 H Et Me 2-OCF₃-4-NO₂ F-727 Me Me Me 2-OCF₃-4-NO₂ F-728 Me Et Me 2-OCF₃-4-NO₂ F-729 Me n-Pr Me 2-OCF₃-4-NO₂ F-730 Me i-Pr Me 2-OCF₃-4-NO₂ F-731 Me n-Bu Me 2-OCF₃-4-NO₂ F-732 Et Et Me 2-OCF₃-4-NO₂ F-733 Et n-Pr Me 2-OCF₃-4-NO₂ F-734 Et i-Pr Me 2-OCF₃-4-NO₂ F-735 n-Pr n-Pr Me 2-OCF₃-4-NO₂ F-736 n-Pr i-Pr Me 2-OCF₃-4-NO₂ F-737 i-Pr i-Pr Me 2-OCF₃-4-NO₂ F-738 H Et Et 2-OCF₃-4-NO₂ F-739 Me Me Et 2-OCF₃-4-NO₂ F-740 Me Et Et 2-OCF₃-4-NO₂ F-741 Me n-Pr Et 2-OCF₃-4-NO₂ F-742 Me i-Pr Et 2-OCF₃-4-NO₂ F-743 Me n-Bu Et 2-OCF₃-4-NO₂ F-744 Et Et Et 2-OCF₃-4-NO₂ F-745 Et n-Pr Et 2-OCF₃-4-NO₂ F-746 Et i-Pr Et 2-OCF₃-4-NO₂ F-747 H CH₂CF₃ H 4-NH₂ F-748 H CH₂CF₃ H 4-NO₂ F-749 H CH₂CF₃ H 2-OMe-4-NH₂ F-750 H CH₂CF₃ H 2-OMe-4-NO₂ F-751 H CH₂CF₃ Me 4-NH₂ F-752 H CH₂CF₃ Me 4-NO₂ F-753 H CH₂CF₃ Me 2-OMe-4-NH₂ F-754 H CH₂CF₃ Me 2-OMe-4-NO₂ F-755 H CH₂CF₃ Et 4-NH₂ F-756 H CH₂CF₃ Et 4-NO₂ F-757 H CH₂CF₃ Et 2-OMe-4-NH₂ F-758 H CH₂CF₃ Et 2-OMe-4-NO₂ F-759 H CH₂CH═CH₂ H 4-NH₂ F-760 H CH₂CH═CH₂ H 4-NO₂ F-761 H CH₂CH═CH₂ H 2-OMe-4-NH₂ F-762 H CH₂CH═CH₂ H 2-OMe-4-NO₂ F-763 H CH₂CH═CH₂ Me 4-NH₂ F-764 H CH₂CH═CH₂ Me 4-NO₂ F-765 H CH₂CH═CH₂ Me 2-OMe-4-NH₂ F-766 H CH₂CH═CH₂ Me 2-OMe-4-NO₂ F-767 H CH₂CH═CH₂ Et 4-NH₂ F-768 H CH₂CH═CH₂ Et 4-NO₂ F-769 H CH₂CH═CH₂ Et 2-OMe-4-NH₂ F-770 H CH₂CH═CH₂ Et 2-OMe-4-NO₂ F-771 H CH₂C≡CH H 4-NH₂ F-772 H CH₂C≡CH H 4-NO₂ F-773 H CH₂C≡CH H 2-OMe-4-NH₂ F-774 H CH₂C≡CH H 2-OMe-4-NO₂ F-775 H CH₂C≡CH Me 4-NH₂ F-776 H CH₂C≡CH Me 4-NO₂ F-777 H CH₂C≡CH Me 2-OMe-4-NH₂ F-778 H CH₂C≡CH Me 2-OMe-4-NO₂ F-779 H CH₂C≡CH Et 4-NH₂ F-780 H CH₂C≡CH Et 4-NO₂ F-781 H CH₂C≡CH Et 2-OMe-4-NH₂ F-782 H CH₂C≡CH Et 2-OMe-4-NO₂ F-783 H CH₂CH₂CF₃ H 4-NH₂ F-784 H CH₂CH₂CF₃ H 4-NO₂ F-785 H CH₂CH₂CF₃ H 2-OMe-4-NH₂ F-786 H CH₂CH₂CF₃ H 2-OMe-4-NO₂ F-787 H CH₂CH₂CF₃ Me 4-NH₂ F-788 H CH₂CH₂CF₃ Me 4-NO₂ F-789 H CH₂CH₂CF₃ Me 2-OMe-4-NH₂ F-790 H CH₂CH₂CF₃ Me 2-OMe-4-NO₂ F-791 H CH₂CH₂CF₃ Et 4-NH₂ F-792 H CH₂CH₂CF₃ Et 4-NO₂ F-793 H CH₂CH₂CF₃ Et 2-OMe-4-NH₂ F-794 H CH₂CH₂CF₃ Et 2-OMe-4-NO₂ F-795 H CH₂CH═CHCH₃ H 4-NH₂ F-796 H CH₂CH═CHCH₃ H 4-NO₂ F-797 H CH₂CH═CHCH₃ H 2-OMe-4-NH₂ F-798 H CH₂CH═CHCH₃ H 2-OMe-4-NO₂ F-799 H CH₂CH═CHCH₃ Me 4-NH₂ F-800 H CH₂CH═CHCH₃ Me 4-NO₂

TABLE 39 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-801 H CH₂CH═CHCH₃ Me 2-OMe-4-NH₂ F-802 H CH₂CH═CHCH₃ Me 2-OMe-4-NO₂ F-803 H CH₂CH═CHCH₃ Et 4-NH₂ F-804 H CH₂CH═CHCH₃ Et 4-NO₂ F-805 H CH₂CH═CHCH₃ Et 2-OMe-4-NH₂ F-806 H CH₂CH═CHCH₃ Et 2-OMe-4-NO₂ F-807 H CH₂C≡CCH₃ H 4-NH₂ F-808 H CH₂C≡CCH₃ H 4-NO₂ F-809 H CH₂C≡CCH₃ H 2-OMe-4-NH₂ F-810 H CH₂C≡CCH₃ H 2-OMe-4-NO₂ F-811 H CH₂C≡CCH₃ Me 4-NH₂ F-812 H CH₂C≡CCH₃ Me 4-NO₂ F-813 H CH₂C≡CCH₃ Me 2-OMe-4-NH₂ F-814 H CH₂C≡CCH₃ Me 2-OMe-4-NO₂ F-815 H CH₂C≡CCH₃ Et 4-NH₂ F-816 H CH₂C≡CCH₃ Et 4-NO₂ F-817 H CH₂C≡CCH₃ Et 2-OMe-4-NH₂ F-818 H CH₂C≡CCH₃ Et 2-OMe-4-NO₂ F-819 Me CH₂CF₃ H 4-NH₂ F-820 Me CH₂CF₃ H 4-NO₂ F-821 Me CH₂CF₃ H 4-OMe-4-NH₂ F-822 Me CH₂CF₃ H 2-OMe-4-NO₂ F-823 Me CH₂CF₃ Me 4-NH₂ F-824 Me CH₂CF₃ Me 4-NO₂ F-825 Me CH₂CF₃ Me 2-OMe-4-NH₂ F-826 Me CH₂CF₃ Me 2-OMe-4-NO₂ F-827 Me CH₂CF₃ Et 4-NH₂ F-828 Me CH₂CF₃ Et 4-NO₂ F-829 Me CH₂CF₃ Et 2-OMe-4-NH₂ F-830 Me CH₂CF₃ Et 2-OMe-4-NO₂ F-831 Me CH₂CH═CH₂ H 4-NH₂ F-832 Me CH₂CH═CH₂ H 4-NO₂ F-833 Me CH₂CH═CH₂ H 2-OMe-4-NH₂ F-834 Me CH₂CH═CH₂ H 2-OMe-4-NO₂ F-835 Me CH₂CH═CH₂ Me 4-NH₂ F-836 Me CH₂CH═CH₂ Me 4-NO₂ F-837 Me CH₂CH═CH₂ Me 2-OMe-4-NH₂ F-838 Me CH₂CH═CH₂ Me 2-OMe-4-NO₂ F-839 Me CH₂CH═CH₂ Et 4-NH₂ F-840 Me CH₂CH═CH₂ Et 4-NO₂ F-841 Me CH₂CH═CH₂ Et 2-OMe-4-NH₂ F-842 Me CH₂CH═CH₂ Et 2-OMe-4-NO₂ F-843 Me CH₂C≡CH H 4-NH₂ F-844 Me CH₂C≡CH H 4-NO₂ F-845 Me CH₂C≡CH H 2-OMe-4-NH₂ F-846 Me CH₂C≡CH H 2-OMe-4-NO₂ F-847 Me CH₂C≡CH Me 4-NH₂ F-848 Me CH₂C≡CH Me 4-NO₂ F-849 Me CH₂C≡CH Me 2-OMe-4-NH₂ F-850 Me CH₂C≡CH Me 2-OMe-4-NO₂ F-851 Me CH₂C≡CH Et 4-NH₂ F-852 Me CH₂C≡CH Et 4-NO₂ F-853 Me CH₂C≡CH Et 2-OMe-4-NH₂ F-854 Me CH₂C≡CH Et 2-OMe-4-NO₂ F-855 Me CH₂CH₂CF₃ H 4-NH₂ F-856 Me CH₂CH₂CF₃ H 4-NO₂ F-857 Me CH₂CH₂CF₃ H 2-OMe-4-NH₂ F-858 Me CH₂CH₂CF₃ H 2-OMe-4-NO₂ F-859 Me CH₂CH₂CF₃ Me 4-NH₂ F-860 Me CH₂CH₂CF₃ Me 4-NO₂ F-861 Me CH₂CH₂CF₃ Me 2-OMe-4-NH₂ F-862 Me CH₂CH₂CF₃ Me 2-OMe-4-NO₂ F-863 Me CH₂CH₂CF₃ Et 4-NH₂ F-864 Me CH₂CH₂CF₃ Et 4-NO₂ F-865 Me CH₂CH₂CF₃ Et 2-OMe-4-NH₂ F-866 Me CH₂CH₂CF₃ Et 2-OMe-4-NO₂ F-867 Me CH₂CH═CHCH₃ H 4-NH₂ F-868 Me CH₂CH═CHCH₃ H 4-NO₂ F-869 Me CH₂CH═CHCH₃ H 2-OMe-4-NH₂ F-870 Me CH₂CH═CHCH₃ H 2-OMe-4-NO₂ F-871 Me CH₂CH═CHCH₃ Me 4-NH₂ F-872 Me CH₂CH═CHCH₃ Me 4-NO₂ F-873 Me CH₂CH═CHCH₃ Me 2-OMe-4-NH₂ F-874 Me CH₂CH═CHCH₃ Me 2-OMe-4-NO₂ F-875 Me CH₂CH═CHCH₃ Et 4-NH₂ F-876 Me CH₂CH═CHCH₃ Et 4-NO₂ F-877 Me CH₂CH═CHCH₃ Et 2-OMe-4-NH₂ F-878 Me CH₂CH═CHCH₃ Et 2-OMe-4-NO₂ F-879 Me CH₂C≡CCH₃ H 4-NH₂ F-880 Me CH₂C≡CCH₃ H 4-NO₂

TABLE 40 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-881 Me CH₂C≡CCH₃ H 2-OMe-4-NH₂ F-882 Me CH₂C≡CCH₃ H 2-OMe-4-NO₂ F-883 Me CH₂C≡CCH₃ Me 4-NH₂ F-884 Me CH₂C≡CCH₃ Me 4-NO₂ F-885 Me CH₂C≡CCH₃ Me 2-OMe-4-NH₂ F-886 Me CH₂C≡CCH₃ Me 2-OMe-4-NO₂ F-887 Me CH₂C≡CCH₃ Et 4-NH₂ F-888 Me CH₂C≡CCH₃ Et 4-NO₂ F-889 Me CH₂C≡CCH₃ Et 2-OMe-4-NH₂ F-890 Me CH₂C≡CCH₃ Et 2-OMe-4-NO₂ F-891 Et CH₂CF₃ H 4-NH₂ F-892 Et CH₂CF₃ H 4-NO₂ F-893 Et CH₂CF₃ H 2-OMe-4-NH₂ F-894 Et CH₂CF₃ H 2-OMe-4-NO₂ F-895 Et CH₂CF₃ Me 4-NH₂ F-896 Et CH₂CF₃ Me 4-NO₂ F-897 Et CH₂CF₃ Me 2-OMe-4-NH₂ F-898 Et CH₂CF₃ Me 2-OMe-4-NO₂ F-899 Et CH₂CF₃ Et 4-NH₂ F-900 Et CH₂CF₃ Et 4-NO₂ F-901 Et CH₂CF₃ Et 2-OMe-4-NH₂ F-902 Et CH₂CF₃ Et 2-OMe-4-NO₂ F-903 Et CH₂CH═CH₂ H 4-NH₂ F-904 Et CH₂CH═CH₂ H 4-NO₂ F-905 Et CH₂CH═CH₂ H 2-OMe-4-NH₂ F-906 Et CH₂CH═CH₂ H 2-OMe-4-NO₂ F-907 Et CH₂CH═CH₂ Me 4-NH₂ F-908 Et CH₂CH═CH₂ Me 4-NO₂ F-909 Et CH₂CH═CH₂ Me 2-OMe-4-NH₂ F-910 Et CH₂CH═CH₂ Me 2-OMe-4-NO₂ F-911 Et CH₂CH═CH₂ Et 4-NH₂ F-912 Et CH₂CH═CH₂ Et 4-NO₂ F-913 Et CH₂CH═CH₂ Et 2-OMe-4-NH₂ F-914 Et CH₂CH═CH₂ Et 2-OMe-4-NO₂ F-915 Et CH₂C≡CH H 4-NH₂ F-916 Et CH₂C≡CH H 4-NO₂ F-917 Et CH₂C≡CH H 2-OMe-4-NH₂ F-918 Et CH₂C≡CH H 2-OMe-4-NO₂ F-919 Et CH₂C≡CH Me 4-NH₂ F-920 Et CH₂C≡CH Me 4-NO₂ F-921 Et CH₂C≡CH Me 2-OMe-4-NH₂ F-922 Et CH₂C≡CH Me 2-OMe-4-NO₂ F-923 Et CH₂C≡CH Et 4-NH₂ F-924 Et CH₂C≡CH Et 4-NO₂ F-925 Et CH₂C≡CH Et 2-OMe-4-NH₂ F-926 Et CH₂C≡CH Et 2-OMe-4-NO₂ F-927 Et CH₂CH₂CF₃ H 4-NH₂ F-928 Et CH₂CH₂CF₃ H 4-NO₂ F-929 Et CH₂CH₂CF₃ H 2-OMe-4-NH₂ F-930 Et CH₂CH₂CF₃ H 2-OMe-4-NO₂ F-931 Et CH₂CH₂CF₃ Me 4-NH₂ F-932 Et CH₂CH₂CF₃ Me 4-NO₂ F-933 Et CH₂CH₂CF₃ Me 2-OMe-4-NH₂ F-934 Et CH₂CH₂CF₃ Me 2-OMe-4-NO₂ F-935 Et CH₂CH₂CF₃ Et 4-NH₂ F-936 Et CH₂CH₂CF₃ Et 4-NO₂ F-937 Et CH₂CH₂CF₃ Et 2-OMe-4-NH₂ F-938 Et CH₂CH₂CF₃ Et 2-OMe-4-NO₂ F-939 Et CH₂CH═CHCH₃ H 4-NH₂ F-940 Et CH₂CH═CHCH₃ H 4-NO₂ F-941 Et CH₂CH═CHCH₃ H 2-OMe-4-NH₂ F-942 Et CH₂CH═CHCH₃ H 2-OMe-4-NO₂ F-943 Et CH₂CH═CHCH₃ Me 4-NH₂ F-944 Et CH₂CH═CHCH₃ Me 4-NO₂ F-945 Et CH₂CH═CHCH₃ Me 2-OMe-4-NH₂ F-946 Et CH₂CH═CHCH₃ Me 2-OMe-4-NO₂ F-947 Et CH₂CH═CHCH₃ Et 4-NH₂ F-948 Et CH₂CH═CHCH₃ Et 4-NO₂ F-949 Et CH₂CH═CHCH₃ Et 2-OMe-4-NH₂ F-950 Et CH₂CH═CHCH₃ Et 2-OMe-4-NO₂ F-951 Et CH₂C≡CCH₃ H 4-NH₂ F-952 Et CH₂C≡CCH₃ H 4-NO₂ F-953 Et CH₂C≡CCH₃ H 2-OMe-4-NH₂ F-954 Et CH₂C≡CCH₃ H 2-OMe-4-NO₂ F-955 Et CH₂C≡CCH₃ Me 4-NH₂ F-956 Et CH₂C≡CCH₃ Me 4-NO₂ F-957 Et CH₂C≡CCH₃ Me 2-OMe-4-NH₂ F-958 Et CH₂C≡CCH₃ Me 2-OMe-4-NO₂ F-959 Et CH₂C≡CCH₃ Et 4-NH₂ F-960 Et CH₂C≡CCH₃ Et 4-NO₂

TABLE 41 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-961  Et CH₂C≡CCH₃ Et 2-OMe-4-NH₂ F-962  Et CH₂C≡CCH₃ Et 2-OMe-4-NO₂ F-963  n-Pr CH₂CF₃ H 4-NH₂ F-964  n-Pr CH₂CF₃ H 4-NO₂ F-965  n-Pr CH₂CF₃ H 2-OMe-4-NH₂ F-966  n-Pr CH₂CF₃ H 2-OMe-4-NO₂ F-967  n-Pr CH₂CF₃ Me 4-NH₂ F-968  n-Pr CH₂CF₃ Me 4-NO₂ F-969  n-Pr CH₂CF₃ Me 2-OMe-4-NH₂ F-970  n-Pr CH₂CF₃ Me 2-OMe-4-NO₂ F-971  n-Pr CH₂CF₃ Et 4-NH₂ F-972  n-Pr CH₂CF₃ Et 4-NO₂ F-973  n-Pr CH₂CF₃ Et 2-OMe-4-NH₂ F-974  n-Pr CH₂CF₃ Et 2-OMe-4-NO₂ F-975  n-Pr CH₂CH═CH₂ H 4-NH₂ F-976  n-Pr CH₂CH═CH₂ H 4-NO₂ F-977  n-Pr CH₂CH═CH₂ H 2-OMe-4-NH₂ F-978  n-Pr CH₂CH═CH₂ H 2-OMe-4-NO₂ F-979  n-Pr CH₂CH═CH₂ Me 4-NH₂ F-980  n-Pr CH₂CH═CH₂ Me 4-NO₂ F-981  n-Pr CH₂CH═CH₂ Me 2-OMe-4-NH₂ F-982  n-Pr CH₂CH═CH₂ Me 2-OMe-4-NO₂ F-983  n-Pr CH₂CH═CH₂ Et 4-NH₂ F-984  n-Pr CH₂CH═CH₂ Et 4-NO₂ F-985  n-Pr CH₂CH═CH₂ Et 2-OMe-4-NH₂ F-986  n-Pr CH₂CH═CH₂ Et 2-OMe-4-NO₂ F-987  n-Pr CH₂C≡CH H 4-NH₂ F-988  n-Pr CH₂C≡CH H 4-NO₂ F-989  n-Pr CH₂C≡CH H 2-OMe-4-NH₂ F-990  n-Pr CH₂C≡CH H 2-OMe-4-NO₂ F-991  n-Pr CH₂C≡CH Me 4-NH₂ F-992  n-Pr CH₂C≡CH Me 4-NO₂ F-993  n-Pr CH₂C≡CH Me 2-OMe-4-NH₂ F-994  n-Pr CH₂C≡CH Me 2-OMe-4-NO₂ F-995  n-Pr CH₂C≡CH Et 4-NH₂ F-996  n-Pr CH₂C≡CH Et 4-NO₂ F-997  n-Pr CH₂C≡CH Et 2-OMe-4-NH₂ F-998  n-Pr CH₂C≡CH Et 2-OMe-4-NO₂ F-999  n-Pr CH₂CH₂CF₃ H 4-NH₂ F-1000 n-Pr CH₂CH₂CF₃ H 4-NO₂ F-1001 n-Pr CH₂CH₂CF₃ H 2-OMe-4-NH₂ F-1002 n-Pr CH₂CH₂CF₃ H 2-OMe-4-NO₂ F-1003 n-Pr CH₂CH₂CF₃ Me 4-NH₂ F-1004 n-Pr CH₂CH₂CF₃ Me 4-NO₂ F-1005 n-Pr CH₂CH₂CF₃ Me 2-OMe-4-NH₂ F-1006 n-Pr CH₂CH₂CF₃ Me 2-OMe-4-NO₂ F-1007 n-Pr CH₂CH₂CF₃ Et 4-NH₂ F-1008 n-Pr CH₂CH₂CF₃ Et 4-NO₂ F-1009 n-Pr CH₂CH₂CF₃ Et 2-OMe-4-NH₂ F-1010 n-Pr CH₂CH₂CF₃ Et 2-OMe-4-NO₂ F-1011 n-Pr CH₂CH═CHCH₃ H 4-NH₂ F-1012 n-Pr CH₂CH═CHCH₃ H 4-NO₂ F-1013 n-Pr CH₂CH═CHCH₃ H 2-OMe-4-NH₂ F-1014 n-Pr CH₂CH═CHCH₃ H 2-OMe-4-NO₂ F-1015 n-Pr CH₂CH═CHCH₃ Me 4-NH₂ F-1016 n-Pr CH₂CH═CHCH₃ Me 4-NO₂ F-1017 n-Pr CH₂CH═CHCH₃ Me 2-OMe-4-NH₂ F-1018 n-Pr CH₂CH═CHCH₃ Me 2-OMe-4-NO₂ F-1019 n-Pr CH₂CH═CHCH₃ Et 4-NH₂ F-1020 n-Pr CH₂CH═CHCH₃ Et 4-NO₂ F-1021 n-Pr CH₂CH═CHCH₃ Et 2-OMe-4-NH₂ F-1022 n-Pr CH₂CH═CHCH₃ Et 2-OMe-4-NO₂ F-1023 n-Pr CH₂C≡CCH₃ H 4-NH₂ F-1024 n-Pr CH₂C≡CCH₃ H 4-NO₂ F-1025 n-Pr CH₂C≡CCH₃ H 2-OMe-4-NH₂ F-1026 n-Pr CH₂C≡CCH₃ H 2-OMe-4-NO₂ F-1027 n-Pr CH₂C≡CCH₃ Me 4-NH₂ F-1028 n-Pr CH₂C≡CCH₃ Me 4-NO₂ F-1029 n-Pr CH₂C≡CCH₃ Me 2-OMe-4-NH₂ F-1030 n-Pr CH₂C≡CCH₃ Me 2-OMe-4-NO₂ F-1031 n-Pr CH₂C≡CCH₃ Et 4-NH₂ F-1032 n-Pr CH₂C≡CCH₃ Et 4-NO₂ F-1033 n-Pr CH₂C≡CCH₃ Et 2-OMe-4-NH₂ F-1034 n-Pr CH₂C≡CCH₃ Et 2-OMe-4-NO₂ F-1035 i-Pr CH₂CF₃ H 4-NH₂ F-1036 i-Pr CH₂CF₃ H 4-NO₂ F-1037 i-Pr CH₂CF₃ H 2-OMe-4-NH₂ F-1038 i-Pr CH₂CF₃ H 2-OMe-4-NO₂ F-1039 i-Pr CH₂CF₃ Me 4-NH₂ F-1040 i-Pr CH₂CF₃ Me 4-NO₂

TABLE 42 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-1041 i-Pr CH₂CF₃ Me 2-OMe-4-NH₂ F-1042 i-Pr CH₂CF₃ Me 2-OMe-4-NO₂ F-1043 i-Pr CH₂CF₃ Et 4-NH₂ F-1044 i-Pr CH₂CF₃ Et 4-NO₂ F-1045 i-Pr CH₂CF₃ Et 2-OMe-4-NH₂ F-1046 i-Pr CH₂CF₃ Et 2-OMe-4-NO₂ F-1047 i-Pr CH₂CH═CH₂ H 4-NH₂ F-1048 i-Pr CH₂CH═CH₂ H 4-NO₂ F-1049 i-Pr CH₂CH═CH₂ H 2-OMe-4-NH₂ F-1050 i-Pr CH₂CH═CH₂ H 2-OMe-4-NO₂ F-1051 i-Pr CH₂CH═CH₂ Me 4-NH₂ F-1052 i-Pr CH₂CH═CH₂ Me 4-NO₂ F-1053 i-Pr CH₂CH═CH₂ Me 2-OMe-4-NH₂ F-1054 i-Pr CH₂CH═CH₂ Me 2-OMe-4-NO₂ F-1055 i-Pr CH₂CH═CH₂ Et 4-NH₂ F-1056 i-Pr CH₂CH═CH₂ Et 4-NO₂ F-1057 i-Pr CH₂CH═CH₂ Et 2-OMe-4-NH₂ F-1058 i-Pr CH₂CH═CH₂ Et 2-OMe-4-NO₂ F-1059 i-Pr CH₂C≡CH H 4-NH₂ F-1060 i-Pr CH₂C≡CH H 4-NO₂ F-1061 i-Pr CH₂C≡CH H 2-OMe-4-NH₂ F-1062 i-Pr CH₂C≡CH H 2-OMe-4-NO₂ F-1063 i-Pr CH₂C≡CH Me 4-NH₂ F-1064 i-Pr CH₂C≡CH Me 4-NO₂ F-1065 i-Pr CH₂C≡CH Me 2-OMe-4-NH₂ F-1066 i-Pr CH₂C≡CH Me 2-OMe-4-NO₂ F-1067 i-Pr CH₂C≡CH Et 4-NH₂ F-1068 i-Pr CH₂C≡CH Et 4-NO₂ F-1069 i-Pr CH₂C≡CH Et 2-OMe-4-NH₂ F-1070 i-Pr CH₂C≡CH Et 2-OMe-4-NO₂ F-1071 i-Pr CH₂CH₂CF₃ H 4-NH₂ F-1072 i-Pr CH₂CH₂CF₃ H 4-NO₂ F-1073 i-Pr CH₂CH₂CF₃ H 2-OMe-4-NH₂ F-1074 i-Pr CH₂CH₂CF₃ H 2-OMe-4-NO₂ F-1075 i-Pr CH₂CH₂CF₃ Me 4-NH₂ F-1076 i-Pr CH₂CH₂CF₃ Me 4-NO₂ F-1077 i-Pr CH₂CH₂CF₃ Me 2-OMe-4-NH₂ F-1078 i-Pr CH₂CH₂CF₃ Me 2-OMe-4-NO₂ F-1079 i-Pr CH₂CH₂CF₃ Et 4-NH₂ F-1080 i-Pr CH₂CH₂CF₃ Et 4-NO₂ F-1081 i-Pr CH₂CH₂CF₃ Et 2-OMe-4-NH₂ F-1082 i-Pr CH₂CH₂CF₃ Et 2-OMe-4-NO₂ F-1083 i-Pr CH₂CH═CHCH₃ H 4-NH₂ F-1084 i-Pr CH₂CH═CHCH₃ H 4-NO₂ F-1085 i-Pr CH₂CH═CHCH₃ H 2-OMe-4-NH₂ F-1086 i-Pr CH₂CH═CHCH₃ H 2-OMe-4-NO₂ F-1087 i-Pr CH₂CH═CHCH₃ Me 4-NH₂ F-1088 i-Pr CH₂CH═CHCH₃ Me 4-NO₂ F-1089 i-Pr CH₂CH═CHCH₃ Me 2-OMe-4-NH₂ F-1090 i-Pr CH₂CH═CHCH₃ Me 2-OMe-4-NO₂ F-1091 i-Pr CH₂CH═CHCH₃ Et 4-NH₂ F-1092 i-Pr CH₂CH═CHCH₃ Et 4-NO₂ F-1093 i-Pr CH₂CH═CHCH₃ Et 2-OMe-4-NH₂ F-1094 i-Pr CH₂CH═CHCH₃ Et 2-OMe-4-NO₂ F-1095 i-Pr CH₂C≡CCH₃ H 4-NH₂ F-1096 i-Pr CH₂C≡CCH₃ H 4-NO₂ F-1097 i-Pr CH₂C≡CCH₃ H 2-OMe-4-NH₂ F-1098 i-Pr CH₂C≡CCH₃ H 2-OMe-4-NO₂ F-1099 i-Pr CH₂C≡CCH₃ Me 4-NH₂ F-1100 i-Pr CH₂C≡CCH₃ Me 4-NO₂ F-1101 i-Pr CH₂C≡CCH₃ Me 2-OMe-4-NH₂ F-1102 i-Pr CH₂C≡CCH₃ Me 2-OMe-4-NO₂ F-1103 i-Pr CH₂C≡CCH₃ Et 4-NH₂ F-1104 i-Pr CH₂C≡CCH₃ Et 4-NO₂ F-1105 i-Pr CH₂C≡CCH₃ Et 2-OMe-4-NH₂ F-1106 i-Pr CH₂C≡CCH₃ Et 2-OMe-4-NO₂

TABLE 43 Compound No. R¹⁵ R¹⁶ R¹⁷ R¹⁸ F-1107 CH₂CF₃ CH₂CF₃ H 4-NH₂ F-1108 CH₂CF₃ CH₂CF₃ H 4-NO₂ F-1109 CH₂CF₃ CH₂CF₃ H 2-OMe-4-NH₂ F-1110 CH₂CF₃ CH₂CF₃ H 2-OMe-4-NO₂ F-1111 CH₂CF₃ CH₂CF₃ Me 4-NH₂ F-1112 CH₂CF₃ CH₂CF₃ Me 4-NO₂ F-1113 CH₂CF₃ CH₂CF₃ Me 2-OMe-4-NH₂ F-1114 CH₂CF₃ CH₂CF₃ Me 2-OMe-4-NO₂ F-1115 CH₂CF₃ CH₂CF₃ Et 4-NH₂ F-1116 CH₂CF₃ CH₂CF₃ Et 4-NO₂ F-1117 CH₂CF₃ CH₂CF₃ Et 2-OMe-4-NH₂ F-1118 CH₂CF₃ CH₂CF₃ Et 2-OMe-4-NO₂ F-1119 CH₂CH═CH₂ CH₂CH═CH₂ H 4-NH₂ F-1120 CH₂CH═CH₂ CH₂CH═CH₂ H 4-NO₂ F-1121 CH₂CH═CH₂ CH₂CH═CH₂ H 2-OMe-4-NH₂ F-1122 CH₂CH═CH₂ CH₂CH═CH₂ H 2-OMe-4-NO₂ F-1123 CH₂CH═CH₂ CH₂CH═CH₂ Me 4-NH₂ F-1124 CH₂CH═CH₂ CH₂CH═CH₂ Me 4-NO₂ F-1125 CH₂CH═CH₂ CH₂CH═CH₂ Me 2-OMe-4-NH₂ F-1126 CH₂CH═CH₂ CH₂CH═CH₂ Me 2-OMe-4-NO₂ F-1127 CH₂CH═CH₂ CH₂CH═CH₂ Et 4-NH₂ F-1128 CH₂CH═CH₂ CH₂CH═CH₂ Et 4-NO₂ F-1129 CH₂CH═CH₂ CH₂CH═CH₂ Et 2-OMe-4-NH₂ F-1130 CH₂CH═CH₂ CH₂CH═CH₂ Et 2-OMe-4-NO₂ F-1131 CH₂C≡CH CH₂C≡CH H 4-NH₂ F-1132 CH₂C≡CH CH₂C≡CH H 4-NO₂ F-1133 CH₂C≡CH CH₂C≡CH H 2-OMe-4-NH₂ F-1134 CH₂C≡CH CH₂C≡CH H 2-OMe-4-NO₂ F-1135 CH₂C≡CH CH₂C≡CH Me 4-NH₂ F-1136 CH₂C≡CH CH₂C≡CH Me 4-NO₂ F-1137 CH₂C≡CH CH₂C≡CH Me 2-OMe-4-NH₂ F-1138 CH₂C≡CH CH₂C≡CH Me 2-OMe-4-NO₂ F-1139 CH₂C≡CH CH₂C≡CH Et 4-NH₂ F-1140 CH₂C≡CH CH₂C≡CH Et 4-NO₂ F-1141 CH₂C≡CH CH₂C≡CH Et 2-OMe-4-NH₂ F-1142 CH₂C≡CH CH₂C≡CH Et 2-OMe-4-NO₂

Test Example 1 Inhibitory Effect Against Cellular Signaling Derived From Ras Oncogene Products

1) Establishment of Cell Lines Used in Assay

Based on the reporter plasmid (pGV-P (Toyo Ink, Japan)), in which luciferase gene was ligated to SV40-derived minimal promoter, we constructed a plasmid designated pRRE3-luc by inserting 3 copies of chemically synthesized oligonucleotides (Sequence: CAGGATATGACTCT, derived from mouse NVL-3 (M. A. Reddy et al.(1992)Mol. Endocrinol., 6, 1051)) into upstream of the promoter. v-ki-ras-transformed NIH3T3 cells (DT cells, provided by Dr. Makoto Noda (Kyoto Univ., School of medicine)) were transfected with this plasmid by liposome-mediated transfection and transfected cell lines stably incorporated and maintained each plasmid were obtained. We named pGV-P and pRRE3-transfected cell line as DT-C and DT-R, respectively and used in the assay described below.

2) Preparation of Samples

i) All the cell lines were cultured in Dulbecco's Modified Essential Medium (DMEM: 10% Fetal Calf Serum(FCS: Hyclone, USA)) including 60 mg/ml kanamycin (Meiji Seika, Japan) in humidified incubator under condition of 5% CO₂ at 37° C.

ii) DT-C and DT-R cells were seeded at 2500 cells/well into flat-bottom 96 well multiplate (Sumitomo bakelite) and incubated for 24 hours.

iii) Test compounds were prepared as 1 mg/ml DMSO solution.

iv) The solution of test compounds were added to the culture. Tested compounds are used at the concentration from 10 mg/ml to 0.51 ng/ml with by 3-fold dilution.

v) After 24 hours, the culture supernatant was completely aspirated and 20 ml of cell-lysing solution (PGC-50 (Toyo Ink, Japan)) was added before cells were dried up. In order to the cells were lysed completely, multiwell plates were left at room temperature for 10 to 30 min. The plates were wrapped up and stored at −20° C. till the day of measurement.

3) Measurement of Samples

i) Melt the samples by putting 96 well multiplate at 37° C. and add 90 μl/well 25 mM Tris (pH 7.5).

ii) Transfer 50 μl of the sample (110 μl) to the 96 well microplate for measurement (Microlite 1 (Dynatech)).

iii) Measure the samples by the luminometer, LUMINOUS CT9000D (Dia-Yatron, Japan). We used Pickagene luminescence kit PGL2000 or LT2.0 (Toyo Ink, Japan) as substrates for luminescence measurement (50 μl/well).

4) Judgment of the Results

i) The luciferase activity of DT-C cells and DT-R cells were plotted in the graph where the relative activity and the compound concentration were expressed as Y-axis and X-axis, respectively. We judged by the degree of dissociation between the activities of DT-C cells and DT-R cells as an index.

ii) Concretely, efficacy of the compound was expressed by two values described below.

a) Among the points of concentration tested, the minimal concentration (Minimal Active Concentration: MAC), at which the activities of DT-C cells and DT-R cells dissociated, was shown as an index of efficacy of the compound. The MAC value was not indicated about the compound which did not show dissociation of both activities in this assay (negative ).

b) Among the points of concentration tested, the concentration which is the nearest to 50% inhibition concentration at DT-C cells (IC50-C), was shown as an index of non-specific transcription-inhibitory effect or of cytotoxicity. In case of positive compounds, 50% inhibition concentration above the area of active concentration in DT-C cells was expressed as IC₅₀-C.

The results of the assay were shown in tables 44 and 45.

TABLE 44 Compound No. MAC (μg/ml) IC₅₀-C (μg/ml) A-1 0.0412 10 A-2 0.0412 10 A-3 0.0412 10 A-23 0.123 10 A-24 0.0137 3.33 A-25 0.370 10 A-26 0.370 >10 A-33 0.0137 >10 A-36 0.0412 3.33 A-37 0.0412 3.33 A-38 0.0412 10 A-40 0.370 10 A-42 0.0137 >10 A-44 <0.000508 3.33 A-49 <0.000508 3.33 A-51 0.123 3.33 A-52 0.123 10 A-57 0.0137 10 A-60 <0.000508 >10 A-61 <0.000508 >10 A-62 0.0412 10 A-63 0.0412 3.33 A-64 0.370 10 A-65 <0.000508 10 A-70 0.123 10 A-71 1.11 10 A-73 0.123 >10 A-74 0.123 10 A-75 <0.000508 >10 A-76 0.0137 10 A-80 0.370 3.33 A-81 0.0412 >10 A-82 <0.000508 10 A-88 0.123 >10 A-89 0.123 >10 A-96 0.370 >10 A-106 0.370 >10 A-107 0.370 10 A-108 0.123 >10 A-110 0.123 >10 A-111 0.123 10 A-112 1.11 >10 A-114 1.11 10 A-119 0.37 >10 A-120 0.123 10 A-121 <0.000508 >10 A-122 1.11 10 A-123 1.11 >10 A-124 0.0137 >10 A-126 0.0137 10 A-127 0.0137 3.33 A-128 0.0412 3.33 A-130 0.123 3.33 A-131 0.0412 >10 A-132 0.123 10 A-133 0.0137 >10 A-134 0.0137 10 A-135 0.0137 10 A-136 0.0137 3.33 A-138 0.0412 1.11 A-139 <0.000508 10 A-140 0.0137 3.33 A-141 0.0412 10 A-142 0.0412 1.11 A-143 0.0412 1.11 A-144 0.0137 >10 A-145 0.0412 >10

TABLE 45 Compound No. MAC (μg/ml) IC₅₀-C (μg/ml) A-146 0.0137 >10 A-147 0.123 >10 A-148 0.123 10 A-149 0.123 3.33 A-150 0.123 10 A-151 0.37 10 A-152 0.123 >10 A-153 0.0412 >10 A-154 0.0412 >10 A-155 0.00457 3.33 A-157 0.0137 >10 A-158 0.0412 >10 A-159 0.0412 10 A-160 0.0137 >10 A-161 0.0412 >10 A-162 0.123 >10 A-163 0.0137 >10 A-164 0.0137 >10 A-165 0.123 10 A-166 0.123 10 A-167 0.0137 10 A-168 0.0412 >10 A-169 0.0412 10 A-170 <0.000508 >10 A-171 0.0137 10 A-172 0.0137 10 A-173 0.123 10 A-174 0.37 >10 A-175 0.0137 3.33 A-176 0.123 10 A-177 0.0412 10 A-178 0.0412 10 A-179 0.0137 10 A-180 0.00457 10 A-181 0.0137 10 A-182 0.0137 3.3 A-183 0.00457 10 A-184 0.0412 10 A-185 0.0137 10 A-186 0.0412 >10 A-187 0.0137 >10 A-188 0.0137 10 A-189 0.0412 10 A-190 0.0412 10 B-2 0.370 10 D-1 1.11 >10 D-6 0.370 >10 D-8 0.0412 >10 D-21 0.37 >10 D-29 1.11 >10 D-30 1.11 >10 D-36 0.0412 >10 D-37 0.123 >10 D-41 1.11 >10 D-45 1.11 10 G-1 0.370 >10

Test Example 2 In Vitro Cell Growth Inhibition Test Cells and MTT Assay

Human squamous lung cancer RERF-RC-AI, human squamous lung cancer Ma44, human lung adenocarcinoma A549, human colon cancer HT29 and human pancreas cancer PANC-1 were used. All cell lines were cultured with Eagle's Modified Essential Medium (EMEM, supplemented with 10% fetal calf serum (FCS: Hyclone, USA) and 60 μg/ml Kanamycin (Meiji-seika, Japan) at 37° C. in a humidified incubator (5% CO₂). The cells were plated in 96-well microcultureplate. Twenty-four hours later, compound were added at the concentration from 10 μg/ml to 0.1 μg/ml with 2-fold dilution. MTT assay was performed 4 days later and IC₅₀ values were determined. The results were shown in Tables 46 to 49 in terms of concentration at ng/ml.

TABLE 46 Compound No. RERF-LC-AI Ma44 A549 HT29 PANC-1 A-1 18 39 22 12 16 A-2 9.0 22 17 15 15 A-3 26 90 35 6.6 15 A-5 200 160 150 A-8 10 12 8 A-9 25 90 100 A-12 870 510 A-18 2.2 A-19 20 A-20 20 A-21 20 A-22 20 A-23 7.8 25 41 A-24 7.1 28 26 A-25 7.8 31 32 A-26 16 55 60 A-27 79 1000 690 A-33 4.0 8.7 12 7.1 7.6 A-36 7.2 26 15 14 A-37 21 240 30 25 A-38 14 34 23 28 A-40 71 49 A-41 65 72 A-42 8.3 49 11 A-44 6.1 18 6.1 160 A-46 140 1800 320 A-49 1.6 3.2 2.8 A-50 47 260 90 A-51 12 88 28 A-52 110 49 24 A-56 850 180 85 A-57 25 14 8.8 A-60 4.0 12 3.9 A-61 4.1 16 6.3 A-62 7.8 24 17 A-63 6.0 53 8.7 A-64 13 86 34 15 30

TABLE 47 Compound No. RERF-LC-AI Ma44 A549 HT29 PANC-1 A-65 1.4 90 2.8 1.4 2.1 A-66 50 1800 36 67 170 A-67 53 6100 83 83 340 A-70 6.7 32 13 8.4 15 A-71 77 310 720 93 180 A-73 12 48 52 16 29 A-74 8 12 34 10 17 A-75 4.0 5.8 8.7 3.8 6.5 A-76 8 100 20 8 16 A-77 30 110 130 44 48 A-78 17 52 63 21 37 A-80 18 62 100 24 50 A-81 9 32 23 7 16 A-82 8 14 31 6 14 A-84 180 410 440 380 300 A-88 20 97 140 43 36 A-89 16 860 150 50 49 A-101 210 790 52 77 A-105 91 110 64 86 A-106 86 82 43 56 A-107 55 65 36 52 A-108 29 27 22 27 A-110 6 63 42 7.7 A-111 17 400 97 35 A-112 23 2000 380 64 A-113 27 1200 620 76 A-114 29 830 320 45 A-115 430 5800 4600 65 A-116 620 4200 3800 72 A-117 160 8600 1100 17 A-119 23 200 1200 100 68 A-120 24 100 1300 23 55 A-121 20 20 58 20 20 A-122 140 300 2100 89 210 A-123 34 90 150 41 A-124 22 24 26 28 A-126 12 170 28 14 A-127 15 17 28 18 17 A-128 36 44 47 42 26

TABLE 48 Compound No. RERF-LC-AI Ma44 A549 HT29 PANC-1 A-129 170 330 430 300 210 A-130 23 39 74 29 18 A-131 15 28 30 25 28 A-132 50 77 180 39 81 A-133 10 15 47 68 15 A-134 16 26 49 13 25 A-135 12 16 52 10 17 A-136 12 16 31 11 16 A-138 43 40 46 30 26 A-139 13 14 13 8 7 A-140 15 47 22 13 12 A-141 16 85 51 32 21 A-142 18 21 38 32 15 A-143 23 33 52 24 20 A-144 7 31 19 6 16 A-145 5 32 90 7 14 A-146 11 52 180 14 24 A-147 8 71 100 8 18 A-148 11 86 490 16 15 A-149 26 85 25 34 41 A-150 16 140 5 31 37 A-151 13 160 70 20 24 A-152 6 39 69 82 13 A-153 11 89 67 15 22 A-154 8 40 12 18 A-155 6 9 80 9 A-156 16 72 23 25 A-157 5 44 8 15 A-158 7 32 25 30 A-161 6.8 7.1 12 5.5 5.3 A-162 8.5 14 28 6.7 9.3 A-165 25 55 95 52 50 A-166 16 49 56 33 28 A-167 3.2 25 12 6.1 6 A-168 2.8 17 12 5.5 5.9 A-169 21 50 41 27 25 A-170 2.7 5.4 14 7.7 6.5 A-171 4 13 12 6.4 6

TABLE 49 Compound No. RERF-LC-AI Ma44 A549 HT29 PANC-1 A-172 1.5 3.8 7.5 3.3 3.1 A-173 3.7 7.2 17 6 7.2 A-174 6.7 76 32 12 14 A-175 5.3 15 17 10 10 A-176 3.2 18 12 6 5.6 A-177 2 4.3 8.2 3.7 3.8 A-178 3.6 24 14 6.7 5 A-179 2 2.6 14 6.3 1.8 A-180 8 16 14 12 8.1 A-181 5.1 6.5 8.7 6.1 5.7 A-182 5.6 16 14 11 7.3 A-183 1.3 2.1 3.9 2 2.6 A-184 2.7 16 10 7.7 3.2 A-185 2.9 6.2 13 6.4 4.1 A-186 14 57 48 14 17 A-187 12 17 25 13 14 A-188 12 16 52 10 17 A-189 16 85 51 32 21 D-2 32 13 D-6 37 320 330 39 85 D-7 83 5200 3200 180 2400 D-8 12 36 27 30 13 D-6 37 320 330 39 85 D-7 83 5200 3200 180 2400 D-8 12 36 27 30 13 D-21 13 350 49 16 D-29 110 520 220 90 D-30 46 2400 100 33 D-32 13 3100 3500 13 D-35 2500 1500 4600 25 D-36 23 65 32 49 D-37 11 24 28 15 13 D-41 24 55 70 40 49 D-42 82 380 570 71 170 D-43 210 200 270 100 100 D-45 62 740 6.1 38 120 G-1 46 56 63 52 51

Test Example 3 Evaluation of in Vivo Antitumor Efficacy

Murine colon cancer Colon 26, human lung cancer RERF-LC-AI and human lung cancer Ma44 were used. Murine- and human-derived tumor cells were maintained by serial transplantation in Balb/c and Balb/c nude mice, respectively. After tumor implantation, compound A-42 suspended in 5% methylcellulose solution were orally administered daily for 14 days. Tumor size (short diameter and long diameter) was scored throughout the experiment and tumor volume was calculated. Antitumor efficacy was evaluated as growth inhibition which was estimated by Treated/Control ratio and shown as % inhibition. Growth inhibition of compound A-42 at 30 mg/kg for 14 days were 70% (P<0.01), 74% (P<0.01) and 66% (P<0.01) against Colon 26 and RERF-LC-AI and Ma44, respectively.

FORMULATION EXAMPLE Formulation Example 1

Granules are prepared using the following ingredients.

Ingredients The compound represented by the formula (I) 10 mg Lactose 700 mg Corn starch 274 mg HPC-L 16 mg 1000 mg

The compound represented by the formula (I) and lactose were made pass through a 60 mesh sieve. Corn starch was made pass through a 120 mesh sieve. They were mixed by a twin shell blender. An aqueous solution of HPC-L (low mucosity hydroxypropylcellulose) was added to the mixture and the resulting mixture was kneaded, granulated (by the extrusion with pore size 0.5 to 1 mm mesh), and dried. The dried granules thus obtained were sieved by a swing sieve (12/60 mesh) to yield the granules.

Formulation 2

Powders for filling capsules are prepared using the following ingredients.

Ingredients The compound represented by the formula (I) 10 mg Lactose 79 mg Corn starch 10 mg Magnesium stearate 1 mg 100 mg

The compound represented by the formula (I) and lactose were made pass through a 60 mesh sieve. Corn starch was made pass through a 120 mesh sieve. These ingredients and magnesium stearate were mixed by a twin shell blender. 100 mg of the 10-fold trituration was filled into a No. 5 hard gelatin capsule.

Formulation 3

Granules for filling capsules are prepared using the following ingredients.

Ingredients The compound represented by the formula (I) 15 mg Lactose 90 mg Corn starch 42 mg HPC-L 3 mg 150 mg

The compound represented by the formula (I) and lactose were made pass through a 60 mesh sieve. Corn starch was made pass through a 120 mesh sieve. After mixing them, an aqueous solution of HPC-L was added to the mixture and the resulting mixture was kneaded, granulated, and dried. After the dried granules were lubricated, 150 mg of that were filled into a No. 4 hard gelatin capsule.

Formulation 4

Tablets are prepared using the following ingredients.

Ingredients The compound represented by the formula (I) 10 mg Lactose 90 mg Microcrystal cellulose 30 mg CMC-Na 15 mg Magnesium stearate 5 mg 150 mg

The compound represented by the formula (I), lactose, niicrocrystal cellulose, and CMC-Na (carboxymethylcellulose sodium salt) were made pass through a 60 mesh sieve and then mixed. The resulting mixture was mixed with magnesium stearate to obtain the mixed powder for the tablet formulation. The mixed powder was compressed to yield tablets of 150 mg.

Industrial Applicability

The pyrimidine derivatives of the present invention have an inhibitory activity against a signal derived from Ras oncogene products, whereby they are effective for solid cancer having high frequency ras activation such as pancreatic cancer, colon cancer, and lung cancer. 

What is claimed is:
 1. A compound represented by the formula (I):

wherein, R¹, R², R³ and R⁴ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, an optionally substituted non-aromatic heterocyclic group, or acyl; or R¹ and R², R³ and R⁴, and R² and R³ each taken together with the adjacent nitrogen atom form the same or different 3- to 6-membered ring optionally containing O, S, or N, provided that R¹ and R², and R³ and R⁴ do not form a ring when R² and R³ taken together form a ring; R⁵ and R⁶ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkyloxy, alkylthio, optionally substituted alkyloxycarbonyl, optionally substituted aryl, optionally substituted heteroaryl, halogen, hydroxy, mercapto, optionally substituted amino, carboxy, cyano, or nitro; X is —N(R⁷)—, —NH—NH—, —O—, or —S— wherein R⁷ is hydrogen atom or optionally substituted alkyl; Y is optionally substituted 5-membered non-aromatic heterocycle-diyl or optionally substituted 5-membered heteroaryl-diyl; Z is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aryl alkenyl, or optionally substituted alkenyl; an ester derivative thereof, an acyloxy derivative thereof or an amide derivative thereof, pharmaceutically acceptable salts thereof, or solvates thereof.
 2. A compound represented by the formula (II):

wherein, R⁸, R⁹, R¹⁰, and R¹¹ are each independently hydrogen atom, optionally substituted alkyl, alkenyl, alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, a non-aromatic heterocyclic group, or acyl; W is —O—, —S—, or —N(R^(A))— wherein R^(A) is hydrogen atom or optionally substituted alkyl; R⁵, R⁶, X and Z are as defined in claim 1, an ester derivative thereof, an acyloxy derivative thereof or an amide derivative thereof, pharmaceutically acceptable salts thereof, or solvates thereof.
 3. A compound represented by the formula (III):

wherein R⁵, R⁶, R⁸, R⁹, R¹⁰, R¹¹, and Z are as defined in claim 2, an ester derivative thereof, an acyloxy derivative thereof or an amide derivative thereof, pharmaceutically acceptable salts thereof, or solvates thereof.
 4. A compound represented by the formula (IV):

wherein R¹² is hydrogen atom or alkyl; V is optionally substituted aryl; R⁸, R⁹, R¹⁰, and R¹¹ are as defined in claim 2, an ester derivative thereof, an acyloxy derivative thereof or an amide derivative thereof, pharmaceutically acceptable salts thereof, or solvates thereof.
 5. The compound of claim 1, an ester derivative thereof, an acyloxy derivative thereof or an amide derivative thereof, pharmaceutically acceptable salts thereof, solvates thereof, wherein R¹, R², R³, and R⁴ are each independently hydrogen atom, optionally substituted alkyl, alkenyl, alkynyl, or acyl.
 6. The compound of claim 1, an ester derivative thereof, an acyloxy derivative thereof or an amide derivative thereof, pharmaceutically acceptable salts thereof, or solvates thereof, wherein R⁸, R⁹, R¹⁰, and R¹¹ are each independently hydrogen atom, optionally substituted alkyl, alkenyl, alkynyl, or acyl.
 7. A pharmaceutical composition comprising a compound of formula 1 as described in claim 1 and a pharmaceutically acceptable carrier.
 8. A method of treating a patient suffering from cancer comprising administering an effective amount of an antitumor agent to a subject comprising a compound of formula (I):

wherein, R¹, R², R³ and R⁴ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, an optionally substituted non-aromatic heterocyclic group, or acyl; or R¹ and R², R³ and R⁴, and R² and R³ each taken together with the adjacent nitrogen atom form the same or different 3- to 6-membered ring optionally containing O, S, or N, provided that R¹ and R², and R³ and R⁴ do not form a ring when R² and R³ taken together form a ring; R⁵ and R⁶ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkyloxy, alkylthio, optionally gubetituted alkyloxycarbonyl, optionally substituted aryl, optionally substituted heteroaryl, halogen, hydroxy, mercapto, optionally substituted amino, carboxy, cyano, or nitro; X is —N(R⁷)—, —NH—NH—, —O—, or —S— wherein R⁷ is hydrogen atom or optionally substituted alkyl; Y is optionally substituted 5-membered non-aromatic heterocycle-diyl or optionally substituted 5-membered heteroaryl-diyl; Z is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aryl alkenyl, or optionally substituted alkenyl; and a pharmaceutically acceptable carrier.
 9. A method of treating a patient suffering from cancer comprising administering an effective amount of a cytostatic agent to a subject comprising a compound of formula

wherein, R¹, R², R³ and R⁴ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, an optionally substituted non-aromatic heterocyclic group, or acyl; or R¹ and R², R³ and R4, and R² and R³ each taken together with the adjacent nitrogen atom form the same or different 3- to 6-membered ring optionally containing O, S, or N, provided that R¹ and R², and R³ and R⁴ do not form a ring when R² and R³ taken together form a ring; R⁵ and R⁶ are each independently hydrogen atom, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted alkyloxy, alkylthio, optionally substituted alkyloxycarbonyl, optionally substituted aryl, optionally substituted heteroaryl, halogen, hydroxy, mercapto, optionally substituted amino, carboxy, cyano, or nitro; X is —N(R⁷)—, —NH—NH—, —O—, or —S— wherein R⁷ is hydrogen atom or optionally substituted alkyl; Y is optionally substituted 5-membered non-aromatic heterocycle-diyl or optionally substituted 5-membered heteroaryl-diyl; Z is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aryl alkenyl, or optionally substituted alkenyl; and a pharmaceutically acceptable carrier.
 10. A method of inhibiting a signal derived from Ras oncogene products comprising administering to a patient an effective amount of the composition of claim 7 and a pharmaceutically acceptable carrier.
 11. A method of alleviating the pathological effects of cancer comprising administering to a patient an effective amount of the composition of claim 7 and a pharmaceutically acceptable carrier.
 12. The method of any one of claims 10 or 11 wherein the agent is administered in an oral or parental dose form.
 13. The method of any one of claims 10 or 11 wherein the composition is administered in an oral or parental dose form. 